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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 649983생성일: 2026년 10월 25일

Thionyl Chloride → N-(2-hydroxy-4-methoxyphenyl)-2-bromo-5-methyl-3-thiophenecarboxamide

https://huagongshe.com/reaction/649983

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물2-Amino-5-methoxyphenolHCID 9942163—
반응물2-Bromo-5-methylthiophene-3-carboxylic acidHCID 11117589—
반응물2-Bromo-5-methyl-3-thiophenecarbonyl chlorideHCID 18422254—
용매PyridineHCID 1049—
용매TolueneHCID 1140—
생성물N-(2-hydroxy-4-methoxyphenyl)-2-bromo-5-methyl-3-thiophenecarboxamideHCID 1086079456.5%

반응 단계

2-Bromo-5-methyl-3-thiophenecarbonyl chloride (2.6 g), prepared in the same manner as above from 2-bromo-5-methyl-3-thiophenecarboxylic acid and thionyl chloride, was suspended in toluene (20 ml). This toluene solution was added dropwise to a solution of 2-amino-5-methoxyphenol (2.0 g) in pyridine (50 ml) at 0° C. The mixture was stirred at room temperature for 2.5 hours and the solvent was evaporated under reduced pressure. The precipitated crystals were collected by filtration, and washed with diluted hydrochloric acid and diisopropyl ether to give N-(2-hydroxy-4-methoxyphenyl)-2-bromo-5-methyl-3-thiophenecarboxamide (2.1 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06271225B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-1c94d5856e89420f893e5855ffbaf56d
출처 메모uspto-grants-2001_08