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HRID 16471作成日:2026年10月26日

Dimethylformamide → p-Acetoxybenzoyl chloride

https://huagongshe.com/reaction/16471

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Benzoic acid, 4-(acetyloxy)-HCID 16865—
反応物Oxalyl chlorideHCID 65578—
溶媒DichloromethaneHCID 6344—
生成物p-Acetoxybenzoyl chlorideHCID 275625499.8%

反応手順

A slurry of 4-acetoxybenzoic acid (100 g, 555.1 mmol) in CH2Cl2 (50 mL) was treated with a catalytic amount of DMF (0.5 mL) and cooled in ice bath. The reaction was stirred as neat oxalyl chloride (51 mL, 582.82 mmol, 1.05 equiv.) was added dropwise. The reaction was allowed to warm to ambient temperature and stirred overnight. The reaction mixture was concentrated under reduced pressure to give 4-(chlorocarbonyl)phenyl acetate (110 g, 100% th.; 110% pract.), which was used in the next step without further purification; 1H NMR (CDCl3) δ 8.09 (d, 2H), 7.20 (d, 2H), 2.28 (s, 3H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737145B2
出典データセットuspto-grants-2010_06
ORD IDord-d168becfdd444e75bda3c5483bb48d6d
出典メモuspto-grants-2010_06