The Reformatsky analogous reaction for the synthesis of novel β-thioxoesters via using aroyl isothiocyanates under solvent-free ball milling and conventional conditions.

The classical Reformatsky reaction, initially described in 1887, is considered one of the most useful ways of forming C-C bonds. The target of this work includes improving the Reformatsky reaction between aroyl isothiocyanates and α-haloesters using metallic zinc to form β-thioxoesters (3-11). In this procedure, a new metal-mediated carbon-carbon linkage is formed with the formation of an organozinc halide and decomposition due to the presence of dilute acid, affording a good yield of the desired product via conventional techniques and ball milling. The Reformatsky reaction requires no solvent and no inert gases. This journal is © The Royal Society of Chemistry.

Introduction

The Reformatsky reaction[1,2] was discovered in 1887 and is still extensively used in the synthesis of heterocyclic compounds because it allows the direct insertion of Zn(0) into α-halogenated esters, and the successive addition of the resulting zinc enolate to ketones, aldehydes, or imines.[3,4] The classical form of the Reformatsky reaction is demonstrated, as shown in Scheme 1A,[5] through the nucleophilic addition of a zinc enolate intermediate to the CO of aldehydes or ketones leading to the formation of a β-hydroxy ester. The essential tool in recent organic synthesis is the formation of C–C bonds. For several reactions this consists of the metal-mediated synthesis of complex organic compounds, where nucleophilic addition to electrophiles has been established. However, the high basicity and/or nucleophilicity of some organometallic reagents limits their utility in late-stage modification, where sensitive functional groups may already be present in the chemical structure. On the other hand, organozinc[6,7] species are a type of “mild” organometallic compound with great functional group compatibility. Conversely,[8] the creation of organozinc species frequently necessitates first gaining access to more reactive organometallics, which are subsequently transmetalized with Zn(ii) salts to yield the necessary organozinc reactant. Activated Zn(0) can also be utilized to make oxidative additions to carbon–halogen bonds[9] (Scheme 1A). Since solvents must often be distilled and dried before use, inert gases are frequently required and, in the case of organozinc reagents, the form of the bulk metal can play an important role, and chemical additives are typically required to generate the activated zinc species, so the formation and manipulation of organometallic compounds are not particularly clean or green.

Scheme 1

(A) The Reformatsky-reaction-based formation of a β-hydroxy ester. (B) The Reformatsky-analogous-reaction-based formation of a β-thioxoester.

Herein, the formation of our target C–C linkage was obtained through the addition of zinc-enolate to the thiocarbonyl group (CS) of isothiocyanate as the starting organic reagents in the Reformatsky reaction, generating the corresponding organozinc species from the reaction of Zn(0) with α-halogenated esters to give a β-thioxoester (Scheme 1B).

Results and discussion

The research began with the treatment of the model substrates, benzoyl isothiocyanate (1)[10-14] (1 mmol) and ethyl 2-bromoacetate (2) (1.5 mmol) with 1 equivalent of zinc (dust <10 mm) heated at 60 °C in benzene (15 ml) for 1–3 h under an N2 atmosphere, as shown in Table 1. The reaction mixture was cooled to 0 °C in ice and then the reaction was quenched with 10% HCl. IR and 1H-NMR spectroscopy of the pure compound confirmed that ethyl 3-benzamido-3-thioxopropanoate (3) was produced in 60% yield (Table 1, entry 1). When the amount of zinc was increased to 1.4 equivalents, the yield of the targeted thioxoester product 3 was greater at 63% (Table 1, entry 2). Adding more zinc with ethyl 2-bromoacetate (2) gave a substantial improvement in yield (Table 1, entries 3–7). With the adjusted reagent ratio in hand, a reaction time study evaluated four different reaction durations of 1, 1.5, 2, and 2.5 h. (Table 1, entries 2 and 5–7), revealing that the reaction requires 2.5 h for complete conversion. The desired product was not produced in a controlled experiment in which zinc was not added to the reaction (Table 1, entry 8).

Optimization of the Reformatsky analogous reaction

Entry	Zn [equiv.]	2 [equiv.]	Solvent	Time [h]	Yield [%]
1	1	1.5	Benzene	2	60
2	1.4	1.5	Benzene	1	63
3	1.8	1.5	Benzene	2	68
4	2	1.5	Benzene	2	68
5	2.4	2.0	Benzene	1.5	70
6	2.8	2.0	Benzene	2	74
7	3	2.0	Benzene	2.5	95
8	0	2.0	Benzene	2.5	0

Then we applied the optimized conditions to another 6 different solvents, as shown in Table 1, entry 7, using a fixed equivalent of zinc : ethyl 2-bromoacetate (3 : 2) for each sample. Luckily, we found that in all cases, regardless of the solvent used, the Reformatsky analogous reaction was successful (Table 2).

Reformatsky analogous reaction using different solvents

Entry	Solvent	Time [h]	Yield [%]
1	Benzene	2.5	95
2	Diethyl ether	2.5	73
3	Toluene	2.5	86
4	Chloroform	2.5	90
5	Dioxane	2.5	83
6	Acetonitrile	2.5	89
7	Tetrahydrofuran	2.5	80

After establishing the optimized conditions, the reactivity with ethyl 2-bromoacetate and zinc (dust <10 mm) under heating was studied (Scheme 2). We found that the Reformatsky analogous reaction showed good functional group tolerance.

Scheme 2

The scope of isothiocyanate electrophiles in the Reformatsky analogous reaction. Reaction conditions: isothiocyanate derivative (1 mmol), ethyl 2-bromoacetate (2 mmol), and zinc (dust, <10 mm, 3 equivalents). Yield refers to the separated products.

The highly hindered substrate 2-chlorobenzoyl isothiocyanate provides the corresponding thioxoester 4 in good yield (72%). Aromatic isothiocyanates were also effective substrates, leading to high yields of isolated products [5–7, 69–81%] (Scheme 2). Under these conditions, the isothiocyanate heterocyclic derivatives were also capable electrophiles, providing isolated products 8 and 9 with 86% and 68% yields, respectively. Aliphatic isothiocyanates such as caproyl and lauroyl isothiocyanates 10 and 11 gave a poor yield of 42% (Scheme 2).

When a solution-based reaction was compared to one performed under ball-milling conditions with comparable chemicals, the convenience of the method was proved (Scheme 3). The solution-based reaction in dry solvent and under a nitrogen atmosphere (N2) at 60 °C with zinc dust yielded 42–95% of the desired products. However, the reaction mixture under ball-milling conditions progressed smoothly without any solvent, inert gas, or additive, giving yields of 50–79% of the desired product (Table 3).

Scheme 3

The Reformatsky analogous reaction with zinc dust under different conditions.

The Reformatsky analogous reaction via the ball-milling technique

Entry	Ar.	Time [h]	Yield [%]
1		4.5	56
2		4	70
3		5	53
4		4.5	76
5		4.5	55
6		4	79
7		4	50
8		5	48
9		5	51

We first compared our mechanochemical technique to the production of such chemicals with a conventional strategy using green metrics, such as atom economy (AE).[15,16] The efficiency with which the atoms in the starting components of a reaction are incorporated into the intended product is referred to as the AE[17] (i.e., how efficiently a reaction makes use of the reactant atoms).[18-20] However, because we employed two different reaction conditions to achieve identical target compounds, the AE values for the mechanochemical and traditional techniques were the same. The theoretical maximum efficiency of reactant usage is given by AE. As a result, we developed yield economy (YE) as a parameter to compare the conversion efficiency of these two different synthetic approaches for the same reaction.[17,21,22] The YE is determined using the following equation: [YE = yield (percent)/reaction time (min)]. It basically evaluates how much yield (percent) of the target product is obtained over a given reaction time. A greater YE indicates a higher conversion rate, a considerably more efficient chemical process, and a more cost-effective reaction. In this study, YE was employed to provide a definitive assessment of yields attained under mechanochemical and conventional settings (Table 4).

Physical data relating to the synthesized target heterocyclic compounds under solvent-free ball-milling and conventional conditionsa

Prod. no.	Time (min)		Yield (%)		Yield (YE) economy (% per min)		AE
	B.M.	Con.	B.M.	Con.	B.M.	Con.
3	270	150	56	95	20.7	63.3	76.0
4	240	150	70	72	29.1	48	78.2
5	300	150	53	73	17.6	48.6	77.8
6	270	150	76	69	28.1	46	80.8
7	270	150	55	81	20.3	54	84.8
8	240	150	79	86	32.9	57.3	75.3
9	240	150	50	68	20.8	45.3	76.4
10	300	150	48	42	16	28	75.9
11	300	150	51	42	17	28	80.6

B.M.: ball milling, Con.: conventional method, AE: atom economy.

Conclusions

The development of an operationally simple one-pot mechanochemical Reformatsky analogous reaction has been completed using isothiocyanate derivatives (CS) instead of aldehydes and/or ketones (CO). This approach eliminates the need for dry solvents, inert gases, and chemical additives via exploiting the organozinc created in situ during milling, resulting in a process with better green metrics.

Experimental

All melting points were determined using uncorrected Griffin and George melting-point equipment (Griffin & George Ltd, Wembley, Middlesex, UK). The quality of the produced compounds was controlled using aluminum sheet silica gel F254 (Merck) thin layer chromatography (TLC). The KBr wafer approach was used to record IR spectra using a Pye Unicam SP1200 spectrophotometer (Pye Unicam Ltd, Cambridge, UK). Ball-milling reactions were made in a MM400 mixer-mill (Retsch GmbH, Haan, Germany), using four 5 mm diameter stainless steel balls in a 5 ml stainless steel jar and were milled vigorously at room temperature with frequency of 1800 rounds per minute (30 Hz). 1H-NMR spectra were obtained on a Bruker Avance III utilizing a Varian Gemini 400 MHz and an internal standard of tetramethylsilane (chemical shifts in scale), whereas 13C-NMR spectra were obtained at 100 MHz in deuterated dimethyl sulfoxide, where TMS was used as an internal standard (DMSO-d6). Elemental studies were performed using a PerkinElmer 2400 CHN elemental analyzer at the Microanalytical Unit, Faculty of Science, Ain Shams University, and satisfactory analytical data (±0.4) were obtained for all substances.

General procedures

Method A: (under inert gas)

A solution of isothiocyanate derivatives 1 (1 mmol) and ethyl 2-bromoacetate (2) (1.5–2.0 mmol) with zinc (dust <10 mm) (3 mmol, 3 equiv.) was reacted under a nitrogen atmosphere (N2) at 60 °C in dry solvent (15 ml) for 1–3 h. The reaction mixture was cooled to 0 °C in ice and then, the reaction was quenched with 10% HCl. The resulting precipitate was separated by filtration and recrystallized from the appropriate solvent to afford a pure compound.

Method B: (ball milling)

A solution of isothiocyanate derivatives 1 (1 mmol) and ethyl 2-bromoacetate (2) (2.0 mmol, 2 equiv.) with zinc (dust <10 mm) (3 mmol, 3 equiv.) was reacted together into a stainless steel jar (5 ml) with four stainless balls (5 mm in diameter). The reaction vessel and another identical vessel were closed and fixed on the vibration arms of the mixer-mill and were vigorously vibrated at room temperature at a rate of 1800 rounds per minute (30 Hz) for 4–5 h. Then the reaction was quenched with 10% HCl. The resulting precipitate was separated by filtration and recrystallized from an appropriate solvent to afford a pure compound.

Ethyl 3-benzamido-3-thioxopropanoate (3)

Pale-yellow crystals; m.p 140–142 °C; IR (KBr) (νmax, cm−1): 3168 (NH), 3021 (CH aromatic), 1713 (COester), 1681 (COamide). 1H-NMR (400 MHz, DMSO-d6) δppm: 1.12 (t, 3H, CH3), 1.72 (q, J = 7.4 Hz, 2H, CH2), 4.89 (s, 2H, CH2), 7.39 (t, J = 8.80 Hz, 1Haromatic), 7.61 (t, J = 4.84 Hz, 2Haromatic), 7.98 (d, J = 1.52 Hz, 2Haromatic), 13.66 (br s, 1H, CONH̲CS, exchangeable with D2O). 13C-NMR (100 MHz, DMSO-d6) δppm: 10, 21, 68, 126, 128, 10, 131, 166, 169, 179. Anal. calcd for C12H13NO3S (251.30) %: C, 57.35; H, 5.21; N, 5.57; found: C, 57.15; H, 5.25; N, 5.60.

Ethyl 3-(2-chlorobenzamido)-3-thioxopropanoate (4)

Yellow crystals; m.p 152–154 °C; IR (KBr) (νmax, cm−1): 3196 (NH), 30 060, 3003 (CH aromatic), 1713 (COester), 1617 (COamide). 1H-NMR (400 MHz, DMSO-d6) δppm: 1.59 (t, J = 8.88 Hz, 3H, CH3), 1.82 (q, J = 7.4 Hz, 2H, CH2), 3.778 (s, 2H, CH2), 6.75 (t, J = 13.12 Hz, 1Haromatic), 6.96 (d, J = 8.16 Hz, 1Haromatic), 7.07 (d, J = 9.6 Hz, 1Haromatic), 7.21 (t, J = 13.36 Hz, 1Haromatic), 10.16 (br s, 1H, CONH̲CS, exchangeable with D2O). 13C-NMR (100 MHz, DMSO-d6) δppm: 20, 22, 70, 127, 128, 129, 137, 146, 155, 159, 171. Anal. Calcd for C12H12ClNO3S (285.74) %: C, 50.44; H, 4.23; N, 4.90; found: C, 50.48; H, 4.28; N, 4.95.

Ethyl 3-cinnamamido-3-thioxopropanoate (5)

White crystals; m.p 222–224 °C; IR (KBr) (νmax, cm−1): 3265 (NH), 3130 (CH aromatic), 1705 (COester), 1688 (COamide). 1H-NMR (400 MHz, DMSO-d6) δppm: 0.67 (t, J = 15.12 Hz, 3H, CH3), 2.14 (q, J = 5.96 Hz, 2H, CH2), 5.13 (s, 2H, CH2), 6.73 (t, J = 14.48 Hz, 1Haromatic), 6.96 (d, J = 8.72 Hz, 2Haromatic), 7.07 (d, J = 7.72 Hz, 1Holiefinic), 7.21 (t, J = 15.68 Hz, 2Haromatic), 7.60 (d, J = 8.72 Hz, 1Holiefinic), 13.75 (br s, 1H, CONH̲CS, exchangeable with D2O). 13C-NMR (100 MHz, DMSO-d6) δppm: 37, 42, 70, 126.03, 126.71, 128.11, 128.46, 128.55, 129.80, 129.89, 167, 170.62, 170.77. Anal. calcd for C14H15NO3S (277.34) %: C, 60.63; H, 5.45; N, 5.05; found: C, 60.60; H, 5.41; N, 5.08.

Ethyl 3-(2-(1,3-dioxoisoindolin-2-yl)acetamido)-3-thioxopropanoate (6)

Yellow crystals; m.p 212–214 °C; IR (KBr) (νmax, cm−1): 3204 (NH), 3063 (CH aromatic), 2921, 2851 (CH aliphatic), 1732 (COester), 1671 (COamide). 1H-NMR (400 MHz, DMSO-d6) δppm: 1.50 (m, 3H, CH3), 1.70 (q, J = 12.72 Hz, 2H, CH2), 4.89 (s, 2H, CSCH̲2CO), 4.92 (s, 2H, NCH̲2CO), 7.38 (m, 2Haromatic), 7.63 (m, 2Haromatic), 13.69 (br s, 1H, CONH̲CS, exchangeable with D2O). 13C-NMR (100 MHz, DMSO-d6) δppm: 15, 22, 65, 66, 123.33, 123.69, 126, 128, 158, 159, 166, 168, 169. Anal. calcd for C15H14N2O5S (334.35) %: C, 53.89; H, 4.22; N, 8.38; found: C, 53.86; H, 4.25; N, 8.35.

Ethyl(E,Z)-3-(2-cyano-3-(1,3-diphenyl-1H-pyrazol-4-yl)acrylamido)-3-thioxopropanoate (7)

Yellow crystals; m.p 278–280 °C; IR (KBr) (νmax, cm−1): 3238 (NH), 3040 (CH aromatic), 2215 (CN), 1712 (COester), 1667 (COamide). 1H-NMR (400 MHz, DMSO-d6) δppm: 1.26 (t, J = 6.08 Hz, 3H, CH3), 4.56 (q, J = 15.20 Hz, 2H, CH2), 5.42 (s, 2H, CSCH̲2CO), 7.55 (m, 3Haromatic), 7.67 (m, 3Haromatic), 7.80 (m, 3Haromatic), 8.02 (m, 2Holiefinic and aromatic), 13.75 (br s, 1H, CONH̲CS, exchangeable with D2O). 13C-NMR (100 MHz, DMSO-d6) δppm: 20, 23, 69, 117, 118, 124.32, 124.78, 129, 131, 132, 135, 141, 153, 167, 170. Anal. calcd for C24H20N4O3S (444.51) %: C, 64.85; H, 4.54; N, 12.60; found: C, 64.82; H, 4.50; N, 12.58.

Ethyl 3-(furan-2-carboxamido)-3-thioxopropanoate (8)

Orange crystals; m.p 148–150 °C; IR (KBr) (νmax, cm−1): 3242 (NH), 3051 (CH aromatic), 1710 (COester), 1669 (COamide). 1H-NMR (400 MHz, DMSO-d6) δppm: 2.19 (m, 3H, CH3), 2.59 (m, 2H, CH2), 4.88 (s, 2H, CSCH̲2CO), 7.61 (dd, J = 7.4 and 1.48 Hz, 1Haromatic), 8.01 (t, J = 7.84 Hz, 1Haromatic), 8.63 (d, J = 8.36 Hz, 1Haromatic), 12.34 (br s, 1H, CONH̲CS, exchangeable with D2O). 13C-NMR (100 MHz, DMSO-d6) δppm: 15, 22, 68, 123.33, 123.69, 126, 128, 158, 159, 168, 169. Anal. calcd for C10H11NO4S (241.26) %: C, 49.78; H, 4.60; N, 5.81; found: C, 49.80; H, 4.64; N, 5.83.

Ethyl 3-(thiophene-2-carboxamido)-3-thioxopropanoate (9)

Yellow crystals; m.p 212–214 °C; IR (KBr) (νmax, cm−1): 3103 (NH), 3053 (CH aromatic), 1730 (COester), 1698 (COamide). 1H-NMR (400 MHz, DMSO-d6) δppm: 1.90 (m, 5H, CH2 and CH3), 4.88 (s, 2H, CSCH̲2CO), 6.69 (dd, J = 6.56 and 7.32 Hz, 1Haromatic), 7.13 (t, J = 15.72 Hz, 1Haromatic), 7.73 (dd, J = 2.36 and 2.52 Hz, 1Haromatic), 12.34 (br s, 1H, CONH̲CS, exchangeable with D2O). 13C-NMR (100 MHz, DMSO-d6) δppm: 19, 21, 68, 112, 118, 129.11, 129.50, 149, 169. Anal. calcd for C10H11NO3S2 (257.32) %: C, 46.68; H, 4.31; N, 5.44; found: C, 46.70; H, 4.28; N, 5.40.

Ethyl 3-hexanamido-3-thioxopropanoate (10)

White crystals; m.p 88–90 °C; IR (KBr) (νmax, cm−1): 3290 (NH), 2922, 2849 (CH aliphatic), 1711 (COester), 1635 (COamide). 1H-NMR (400 MHz, DMSO-d6) δppm: 0.88 (t, J = 10.96 Hz, 3H, OCH2CH̲3), 1.26 (m, 3Haliphatic), 1.38 (m, 4Haliphatic), 1.64 (m, 4Haliphatic), 4.75 (s, 2H, CSCH̲2CO), 5.16 (q, J = 15.20 Hz, 2H, OCH̲2CH3), 13.69 (br s, 1H, CONH̲CS, exchangeable with D2O). 13C-NMR (100 MHz, DMSO-d6) δppm: 28, 29.29, 29.36, 29.41, 29.60, 29.61, 30, 31, 68, 152, 166, 169. Anal. calcd for C11H19NO3S (245.34) %: C, 53.85; H, 7.81; N, 5.71; found: C, 53.88; H, 7.85; N, 5.73.

Ethyl 3-dodecanamido-3-thioxopropanoate (11)

White crystals; m.p 78–80 °C; IR (KBr) (νmax, cm−1): 3171 (NH), 2917, 2849 (CH aliphatic), 1700 (br COester), 1679 (COamide). 1H-NMR (400 MHz, DMSO-d6) δppm: 1.05 (m, 6Haliphatic), 1.56 (m, 20Haliphatic), 3.62 (m, 2H, OCH̲2CH3), 5.01 (s, 2H, CSCH̲2CO), 12.89 (br s, 1H, CONH̲CS, exchangeable with D2O). 13C-NMR (100 MHz, DMSO-d6) δppm: 22, 26, 28, 29.29, 29.36, 29.41, 29.60, 29.61, 30, 31, 65, 161, 169.13, 169.70. Anal. calcd for C17H31NO3S (329.50) %: C, 61.97; H, 9.48; N, 4.25; found: C, 61.95; H, 9.44; N, 4.18.

Conflicts of interest

The authors declare no competing financial interests.