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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 452571생성일: 2026년 10월 24일

Dimethylformamide → N-methoxy-N-methyl-3-(trifluoromethoxy)benzamide

https://huagongshe.com/ko/reaction/452571

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물N,O-DimethylhydroxylamineHCID 14232—
반응물Oxalyl chlorideHCID 65578—
반응물3-(Trifluoromethoxy)benzoic acidHCID 66096—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-methoxy-N-methyl-3-(trifluoromethoxy)benzamideHCID 8665640680%

반응 단계

To a stirred solution of 3-(trifluoromethoxy)benzoic acid (20.0 g, 96.1 mmol) in dichloromethane (200 mL), cooled to 0° C. with a brine/ice bath, was added N,N-dimethylformamide (0.37 mL, 4.8 mmol) followed by oxalyl chloride (10.1 mL, 115 mmol). The resulting mixture was stirred 5 h at room temperature, until gas evolution stopped and a clear solution was obtained. The mixture was cooled to 0° C. with a brine/ice bath, N,O-Dimethylhydroxylamine (9.37 g, 96 mmol) was added at once, followed by dropwise addition of triethylamine (45.5 mL, 326 mmol) through a dropping funnel, while keeping the internal temperature below 10° C. The resulting suspension was diluted with dichloromethane (200 mL), stirred overnight at room temperature, poured into water (400 mL) and the aqueous layer was extracted with dichloromethane (2×150 mL). The organic layers were combined, washed with water (2×200 mL), dried (MgSO4), and concentrated in vacuo. The residue was purified over silica gel to afford N-methoxy-N-methyl-3-(trifluoromethoxy)benzamide as an oil [22.4 g, yield 80%; HPLC/MS:m/z=250 (M+H); log P(HCOOH)=2.41].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492388B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-d469d57969fc44258056934f99627f38
출처 메모uspto-grants-2013_07