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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1625772생성일: 2026년 10월 25일

Triethylamine → 5-bromo-N-methoxy-N,2-dimethylbenzamide

https://huagongshe.com/reaction/1625772

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물5-Bromo-2-methylbenzoyl chlorideHCID 22328611—
용매DichloromethaneHCID 6344—
생성물5-bromo-N-methoxy-N,2-dimethylbenzamideHCID 65307193—

반응 단계

The above 5-bromo-2-methylbenzoic acid (10.0 g) was suspended in dichloromethane (100 ml), and thereto were added oxalyl chloride (8.1 ml) and N,N-dimethylformamide (2 drops). The mixture was stirred at room temperature for 4 hours. The solvent was evaporated under reduced pressure to give 5-bromo-2-methylbenzoyl chloride. This benzoyl chloride was dissolved in dichloromethane (200 ml), and thereto was added N,O-dimethylhydroxylamine hydrochloride (12.3 g). To the mixture was added dropwise triethylamine (20 ml) at 0° C., and the mixture was stirred at room temperature overnight. The solvent was evaporated under reduced pressure, and the residue was extracted with ethyl acetate, and washed successively with water, 10% aqueous hydrochloric acid solution, water, a saturated aqueous sodium hydrogen carbonate solution, and brine. The extract was dried over sodium sulfate, and the solvent was evaporated under reduced pressure to give N-methoxy-N-methyl-5-bromo-2-methylbenzamide (12.25 g) as oil. APCI-Mass m/Z 258/260 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08785403B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-8427aad2ded1492f8e5761eada88c021
출처 메모uspto-grants-2014_07