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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30554생성일: 2026년 10월 24일

Benzoyl chloride, 3-bromo- → 3-Bromo-N-methoxy-N-methylbenzamide

https://huagongshe.com/ko/reaction/30554

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chloride, 3-bromo-HCID 74377—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물DiisopropylethylamineHCID 81531—
용매DichloromethaneHCID 6344—
생성물3-Bromo-N-methoxy-N-methylbenzamideHCID 1216287590.3%

반응 단계

A mixture of N-methoxymethanamine hydrochloride (22.1 g, 228.5 mmol), diisopropyl ethyl amine (63.5 mL, 365.6 mmol) and CH2Cl2 was treated dropwise with 3-bromobenzoyl chloride (15 g, 68.5 mmol) in CH2Cl2, stirred at room temperature for 30 minutes, and concentrated under vacuum. The resultant residue was dispersed in water and extracted with ethyl ether. The organic extracts were combined, dried over MgSO4 and concentrated in vacuo. The resultant residue was purified on silica gel (Biotage) using hexanes/EtOAc (2/1) as the eluting solvents to give 3-bromo-N-methoxy-N-methylbenzamide as a tan solid (15.1 g, 90% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423158B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-166da1d9e33a4bd8acda9bd0700ddbfe
출처 메모uspto-grants-2008_09