(2-Chloro-8-methyl-quinolin-3-yl)methanol.

The mol-ecule of title compound, C(11)H(10)ClNO, is close to being planar (r.m.s deviation for the non-H atoms = 0.017 Å). In the crystal, mol-ecules inter-act by way of O-H⋯O hydrogen bonds, generating C(2) chains propagating in [010]. The crystal structure is consolidated by C-H⋯π inter-actions and aromatic π-π stacking inter-actions [centroid-centroid distance = 3.661 (2) Å].

Related literature

For a related structure and background references, see: Roopan et al. (2010 ▶). For a similar structure, see: Khan et al. (2009 ▶).

Experimental

Crystal data

C11H10ClNO

M = 207.65

Monoclinic,

a = 14.963 (2) Å

b = 4.632 (1) Å

c = 14.469 (2) Å

β = 103.612 (1)°

V = 974.7 (3) Å3

Z = 4

Mo Kα radiation

μ = 0.35 mm−1

T = 290 K

0.40 × 0.24 × 0.11 mm

Data collection

Oxford Xcalibur Eos(Nova) CCD detector diffractometer

Absorption correction: multi-scan (CrysAlis PRO RED; Oxford Diffraction, 2009 ▶) T min = 0.871, T max = 0.962

7607 measured reflections

1723 independent reflections

790 reflections with I > 2σ(I)

R int = 0.167

Refinement

R[F 2 > 2σ(F 2)] = 0.061

wR(F 2) = 0.135

S = 0.85

1723 reflections

129 parameters

H-atom parameters constrained

Δρmax = 0.23 e Å−3

Δρmin = −0.23 e Å−3

Data collection: CrysAlis PRO CCD (Oxford Diffraction, 2009 ▶); cell refinement: CrysAlis PRO CCD; data reduction: CrysAlis PRO RED (Oxford Diffraction, 2009 ▶); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: ORTEP-3 (Farrugia, 1997 ▶); software used to prepare material for publication: WinGX (Farrugia, 1999 ▶).

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536810020490/hb5470sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536810020490/hb5470Isup2.hkl

Additional supplementary materials: crystallographic information; 3D view; checkCIF report

C11H10ClNO	F(000) = 432
Mr = 207.65	Dx = 1.415 Mg m−3
Monoclinic, P21/c	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybc	Cell parameters from 972 reflections
a = 14.963 (2) Å	θ = 2.0–20.5°
b = 4.632 (1) Å	µ = 0.35 mm−1
c = 14.469 (2) Å	T = 290 K
β = 103.612 (1)°	Plate, colourless
V = 974.7 (3) Å3	0.40 × 0.24 × 0.11 mm
Z = 4

Oxford Xcalibur Eos(Nova) CCD detector diffractometer	1723 independent reflections
Radiation source: Enhance (Mo) X-ray Source	790 reflections with I > 2σ(I)
graphite	Rint = 0.167
ω scans	θmax = 25.0°, θmin = 2.9°
Absorption correction: multi-scan (CrysAlis PRO RED; Oxford Diffraction, 2009)	h = −17→17
Tmin = 0.871, Tmax = 0.962	k = −5→5
7607 measured reflections	l = −17→17

Refinement on F2	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.061	Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.135	H-atom parameters constrained
S = 0.85	w = 1/[σ2(Fo2) + (0.0492P)2] where P = (Fo2 + 2Fc2)/3
1723 reflections	(Δ/σ)max < 0.001
129 parameters	Δρmax = 0.23 e Å−3
0 restraints	Δρmin = −0.23 e Å−3

Geometry. Bond distances, angles etc. have been calculated using the rounded fractional coordinates. All su's are estimated from the variances of the (full) variance-covariance matrix. The cell e.s.d.'s are taken into account in the estimation of distances, angles and torsion angles

Refinement. Refinement on F2 for ALL reflections except those flagged by the user for potential systematic errors. Weighted R-factors wR and all goodnesses of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The observed criterion of F2 > σ(F2) is used only for calculating -R-factor-obs etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R-factors based on ALL data will be even larger.

	x	y	z	Uiso*/Ueq
Cl1	0.13301 (8)	0.6900 (2)	−0.03546 (7)	0.0599 (5)
O1	0.0342 (2)	0.8800 (5)	0.2237 (2)	0.0534 (11)
N1	0.2487 (2)	0.3588 (7)	0.0784 (2)	0.0372 (11)
C1	0.1808 (3)	0.5392 (8)	0.0749 (2)	0.0368 (14)
C2	0.1436 (3)	0.6216 (7)	0.1526 (3)	0.0340 (14)
C3	0.1835 (3)	0.4990 (8)	0.2376 (3)	0.0398 (16)
C4	0.2981 (3)	0.1674 (9)	0.3335 (3)	0.0475 (17)
C5	0.3681 (3)	−0.0242 (10)	0.3370 (3)	0.0551 (17)
C6	0.3985 (3)	−0.0855 (9)	0.2554 (3)	0.0538 (17)
C7	0.3611 (3)	0.0351 (9)	0.1686 (3)	0.0427 (17)
C8	0.2875 (3)	0.2323 (8)	0.1643 (3)	0.0365 (12)
C9	0.2566 (3)	0.3003 (8)	0.2465 (3)	0.0369 (14)
C10	0.0635 (3)	0.8293 (8)	0.1397 (3)	0.0436 (16)
C11	0.3954 (3)	−0.0328 (10)	0.0817 (3)	0.0589 (17)
H1O	0.00970	0.73400	0.23830	0.0800*
H3	0.16230	0.54700	0.29100	0.0480*
H4	0.27790	0.20970	0.38810	0.0570*
H5	0.39560	−0.11390	0.39410	0.0660*
H6	0.44670	−0.21540	0.26010	0.0640*
H10A	0.08110	1.01170	0.11630	0.0520*
H10B	0.01230	0.75250	0.09200	0.0520*
H11A	0.44600	−0.16520	0.09810	0.0880*
H11B	0.41540	0.14190	0.05710	0.0880*
H11C	0.34680	−0.11840	0.03440	0.0880*

	U11	U22	U33	U12	U13	U23
Cl1	0.0614 (8)	0.0749 (9)	0.0457 (7)	0.0113 (7)	0.0170 (6)	0.0132 (6)
O1	0.060 (2)	0.0369 (17)	0.078 (2)	0.0016 (16)	0.0457 (18)	−0.0011 (16)
N1	0.042 (2)	0.035 (2)	0.0375 (19)	−0.0031 (18)	0.0153 (17)	−0.0004 (17)
C1	0.044 (3)	0.031 (2)	0.037 (2)	−0.007 (2)	0.013 (2)	−0.0008 (19)
C2	0.040 (3)	0.028 (2)	0.037 (2)	−0.005 (2)	0.015 (2)	−0.003 (2)
C3	0.044 (3)	0.043 (3)	0.039 (2)	−0.009 (2)	0.023 (2)	−0.006 (2)
C4	0.051 (3)	0.052 (3)	0.042 (3)	−0.010 (3)	0.016 (2)	0.000 (2)
C5	0.053 (3)	0.063 (3)	0.047 (3)	−0.004 (3)	0.007 (2)	0.012 (2)
C6	0.038 (3)	0.051 (3)	0.071 (3)	−0.001 (2)	0.010 (3)	0.011 (3)
C7	0.037 (3)	0.044 (3)	0.048 (3)	−0.006 (2)	0.012 (2)	0.002 (2)
C8	0.037 (2)	0.036 (2)	0.038 (2)	−0.007 (2)	0.012 (2)	−0.002 (2)
C9	0.043 (3)	0.036 (2)	0.034 (2)	−0.007 (2)	0.014 (2)	−0.003 (2)
C10	0.046 (3)	0.038 (2)	0.053 (3)	−0.004 (2)	0.024 (2)	−0.002 (2)
C11	0.050 (3)	0.069 (3)	0.063 (3)	0.010 (3)	0.024 (2)	−0.006 (3)

Cl1—C1	1.735 (3)	C7—C11	1.499 (6)
O1—C10	1.406 (5)	C7—C8	1.421 (6)
O1—H1O	0.8200	C8—C9	1.409 (6)
N1—C8	1.373 (5)	C3—H3	0.9300
N1—C1	1.307 (5)	C4—H4	0.9300
C1—C2	1.419 (6)	C5—H5	0.9300
C2—C10	1.514 (6)	C6—H6	0.9300
C2—C3	1.359 (6)	C10—H10A	0.9700
C3—C9	1.412 (6)	C10—H10B	0.9700
C4—C9	1.408 (6)	C11—H11A	0.9600
C4—C5	1.365 (6)	C11—H11B	0.9600
C5—C6	1.391 (6)	C11—H11C	0.9600
C6—C7	1.368 (6)
C10—O1—H1O	110.00	O1—C10—C2	113.5 (3)
C1—N1—C8	117.8 (3)	C2—C3—H3	119.00
Cl1—C1—N1	116.2 (3)	C9—C3—H3	119.00
Cl1—C1—C2	117.9 (3)	C5—C4—H4	120.00
N1—C1—C2	126.0 (3)	C9—C4—H4	120.00
C1—C2—C3	115.7 (4)	C4—C5—H5	120.00
C1—C2—C10	121.3 (4)	C6—C5—H5	120.00
C3—C2—C10	122.9 (4)	C5—C6—H6	118.00
C2—C3—C9	121.4 (4)	C7—C6—H6	118.00
C5—C4—C9	119.4 (4)	O1—C10—H10A	109.00
C4—C5—C6	120.2 (4)	O1—C10—H10B	109.00
C5—C6—C7	123.4 (4)	C2—C10—H10A	109.00
C6—C7—C11	122.5 (4)	C2—C10—H10B	109.00
C8—C7—C11	120.9 (4)	H10A—C10—H10B	108.00
C6—C7—C8	116.6 (4)	C7—C11—H11A	109.00
N1—C8—C9	121.0 (4)	C7—C11—H11B	109.00
C7—C8—C9	120.8 (4)	C7—C11—H11C	109.00
N1—C8—C7	118.2 (4)	H11A—C11—H11B	109.00
C3—C9—C4	122.4 (4)	H11A—C11—H11C	109.00
C4—C9—C8	119.6 (4)	H11B—C11—H11C	110.00
C3—C9—C8	118.0 (4)
C8—N1—C1—Cl1	−179.2 (3)	C9—C4—C5—C6	0.5 (7)
C8—N1—C1—C2	1.0 (6)	C5—C4—C9—C3	179.6 (4)
C1—N1—C8—C7	179.8 (4)	C5—C4—C9—C8	0.4 (6)
C1—N1—C8—C9	−1.5 (6)	C4—C5—C6—C7	−0.7 (7)
Cl1—C1—C2—C3	−179.7 (3)	C5—C6—C7—C8	0.0 (7)
Cl1—C1—C2—C10	1.3 (5)	C5—C6—C7—C11	179.6 (4)
N1—C1—C2—C3	0.1 (6)	C6—C7—C8—N1	179.6 (4)
N1—C1—C2—C10	−178.9 (4)	C6—C7—C8—C9	0.9 (6)
C1—C2—C3—C9	−0.7 (6)	C11—C7—C8—N1	0.0 (6)
C10—C2—C3—C9	178.3 (4)	C11—C7—C8—C9	−178.7 (4)
C1—C2—C10—O1	178.4 (3)	N1—C8—C9—C3	1.0 (6)
C3—C2—C10—O1	−0.6 (5)	N1—C8—C9—C4	−179.8 (4)
C2—C3—C9—C4	−179.1 (4)	C7—C8—C9—C3	179.7 (4)
C2—C3—C9—C8	0.1 (6)	C7—C8—C9—C4	−1.1 (6)

Cg1 is a centroid of the N1/C1–C3/C8/C9 ring.

D—H···A	D—H	H···A	D···A	D—H···A
O1—H1O···O1i	0.82	1.90	2.712 (4)	174
C10—H10A···Cg1ii	0.97	2.75	3.557 (4)	141

Table 1

Hydrogen-bond geometry (Å, °)

Cg1 is a centroid of the N1/C1–C3/C8/C9 ring.

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O1—H1O⋯O1i	0.82	1.90	2.712 (4)	174
C10—H10A⋯Cg1ii	0.97	2.75	3.557 (4)	141

Symmetry codes: (i) ; (ii) .