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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7735생성일: 2026년 10월 25일

2-Aminophenol → 3,5-dimethoxy-N-(2-methoxyphenyl)-4-methylbenzamide

https://huagongshe.com/reaction/7735

반응식

참여 물질

역할이름HCID투입량
반응물2-AminophenolHCID 5801—
반응물Thionyl ChlorideHCID 24386—
반응물DiisopropylethylamineHCID 81531—
반응물3,5-Dimethoxy-4-methylbenzoic acidHCID 3764486—
용매TetrahydrofuranHCID 8028—
생성물3,5-dimethoxy-N-(2-methoxyphenyl)-4-methylbenzamideHCID 2599339—

반응 단계

Thionyl chloride (10 mL) and 3,5-dimethoxy-4-methylbenzoic acid (1.0 g, 5.1 mmol) was refluxed under argon until no starting material was observed by TLC. After cooling reaction mixture to rt, concentrated mixture in vacuo. The resulting brown oil was added to a mixture of 2-aminophenol (580 mg, 5.3 mmol), diisopropylethyl amine (1.1 mL, 6.3 mmol) and THF (40 mL) at 0° C. and then brought to rt overnight. After concentrating mixture in vacuo, the resulting brown oil was purified by flash chromatography on silica gel, using a gradient elution from 1:9 EtOAc:hexanes to 1:1 EtOAc:hexanes. This afforded the desired intermediate, 3,5-dimethoxy-N-(2-methoxyphenyl)-4-methylbenzamide, as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6aab020e505c4013a9621c93cb7e9ea8
출처 메모uspto-grants-2006_08