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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7687생성일: 2026년 10월 23일

2-Aminophenol → 3-bromo-N-(2-hydroxyphenyl)4-methylbenzamide

https://huagongshe.com/ko/reaction/7687

반응식

참여 물질

역할이름HCID투입량
반응물2-AminophenolHCID 5801—
반응물Thionyl ChlorideHCID 24386—
반응물DiisopropylethylamineHCID 81531—
반응물3-Bromo-4-methylbenzoic acidHCID 82130—
용매TetrahydrofuranHCID 8028—
생성물3-bromo-N-(2-hydroxyphenyl)4-methylbenzamideHCID 21990965—

반응 단계

A mixture of 3-bromo-4-methylbenzoic acid (1.0 g, 4.7 mmol) and thionyl chloride (18 mL) was refluxed for 1 h and then cooled to rt. The excess thionyl chloride was removed int vacuo, the residue was dissolved in THF (10 mL), and it was added to a cooled (0° C.) mixture of 2-aminophenol (507 mg, 4.7 mmol) and diisopropylethylamine (0.90 mL; 5.1 mmol) in THF (18 mL). The resulting mixture was stirred at rt for 4 h. The solvent was then removed and the residue was purified by flash chromatography on silica gel eluting with EtOAc:hexanes (1:5 to 1:4) to afford 3-bromo-N-(2-hydroxyphenyl)-4-methylbenzamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-8c9853080e9e4c4981f9fefb9aec9e45
출처 메모uspto-grants-2006_08