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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19675생성일: 2026년 10월 24일

1,2-Dichloroethane → 2-Amino-5-fluoro-N-methoxy-N-methylbenzamide

https://huagongshe.com/ko/reaction/19675

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물DiisopropylethylamineHCID 81531—
반응물2-Amino-5-fluorobenzoic acidHCID 101412—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물2-Amino-5-fluoro-N-methoxy-N-methylbenzamideHCID 53407572—

반응 단계

To a 0° C. mixture of diisopropylethylamine (34.36 mL, 197.25 mmol) and O,N-dimethyl-hydroxylamine hydrochloride (19.24 g, 197.25 mmol) in CHCl3 (300 mL) was added 2-amino-5-fluorobenzoic acid (25.50 g, 164.38 mmol) followed by EDC (31.51 g, 164.38 mmol). The reaction was stirred from 0° C. to ambient temperature over 2 h and then diluted with CH2Cl2 (100 mL), washed with saturated sodium bicarbonate solution (100 mL) and brine (100 mL), dried over Na2SO4, filtered, and concentrated in vacuo. Purification by normal phase chromatography (3-8% MeOH/CH2Cl2) yielded 2-amino-5-fluoro-N-methoxy-N-methylbenzamide as a yellow oil. 1H NMR (CDCl3, 400 MHz) 7.12 (m, 1H, ArH); 6.93 (m, 1H, ArH); 6.65 (m, 1H, ArH); 3.63 (s, 3H, CH3); 3.35 (s, 3H, CH3); MS (Electrospray): m/z 199.1 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745452B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3d66f49508da4beb9babdb20a9d84317
출처 메모uspto-grants-2010_06