Literature DB >> 18981622

Catalytic hypervalent iodine oxidation of p-dialkoxybenzenes to p-quinones using 4-iodophenoxyacetic acid and Oxone.

Takayuki Yakura1, Yû Yamauchi, Yuan Tian, Masanori Omoto.   

Abstract

A catalytic hypervalent iodine oxidation of p-dialkoxybenzenes using 4-iodophenoxyacetic acid (1) and 2KHSO5 x KHSO4 x K2SO4 (Oxone) was developed. Reaction of p-dialkoxybenzenes (2) with a catalytic amount of 1 in the presence of Oxone as a co-oxidant in 2,2,2-trifluoroethanol-water (1 : 2) gave the corresponding p-quinones (3) in excellent yields without purification. This procedure was applied to synthesis of blattellaquinone (9), the sex pheromone of the German cockroach, Blattella germanica.

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Year:  2008        PMID: 18981622     DOI: 10.1248/cpb.56.1632

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  3 in total

1.  2-Iodo-N-isopropyl-5-methoxybenzamide as a highly reactive and environmentally benign catalyst for alcohol oxidation.

Authors:  Takayuki Yakura; Tomoya Fujiwara; Akihiro Yamada; Hisanori Nambu
Journal:  Beilstein J Org Chem       Date:  2018-04-30       Impact factor: 2.883

2.  IBS-catalyzed regioselective oxidation of phenols to 1,2-quinones with Oxone®.

Authors:  Muhammet Uyanik; Tatsuya Mutsuga; Kazuaki Ishihara
Journal:  Molecules       Date:  2012-07-18       Impact factor: 4.411

3.  Practical Synthesis of 2-Iodosobenzoic Acid (IBA) without Contamination by Hazardous 2-Iodoxybenzoic Acid (IBX) under Mild Conditions.

Authors:  Hideyasu China; Nami Kageyama; Hotaka Yatabe; Naoko Takenaga; Toshifumi Dohi
Journal:  Molecules       Date:  2021-03-27       Impact factor: 4.411

  3 in total

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