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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1987992생성일: 2026년 10월 24일

Acetyl chloride → 2-Methyl-1,3-benzoxazole-4-carboxylic acid

https://huagongshe.com/ko/reaction/1987992

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물TriethylamineHCID 8471—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물2-Amino-3-hydroxybenzoic acid hydrobromideHCID 66880740—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2-Methyl-1,3-benzoxazole-4-carboxylic acidHCID 1835462864%

반응 단계

To a mixture of 2-amino-3-hydroxybenzoic acid hydrobromide (0.35 g, 1.50 mmol) and acetyl chloride (0.11 mL, 1.50 mmol) in dichloromethane (10 mL) was added triethylamine (0.84 mL, 6.0 mmol) dropwise, then the reaction mixture was stirred at room temperature for 12 h. The reaction mixture was diluted with dichloromethane, and then washed with 2 N HCl. The aqueous layer was extracted with dichloromethane. The combined organic layers were washed with brine, dried (Na2SO4), filtered and concentrated. The crude product was dissolved in toluene (10 mL) and the solution was treated with p-toluenesulfonic acid monohydrate (263 mg, 1.38 mmol). The reaction mixture was then heated to reflux for 1.5 h. The reaction was cooled to room temperature, poured into water and extracted with ethyl acetate. The organic layer was separated then washed with water, brine, dried (Na2SO4), filtered and concentrated. The crude product was purified by column chromatography (silica gel, 9:1 to 3:1 ethyl acetate/methanol) to afford 2-methylbenzoxazole-4-carboxylic acid (0.17 g, 64%) as an off-white solid: MS (ESI+) m/z 178 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07553846B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-20f3a9151b214a2dae58ea1923ec61a8
출처 메모uspto-grants-2009_06