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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 274477생성일: 2026년 10월 25일

Boron tribromide → 2-Bromo-1-(3,4-dihydroxy-5-nitro-phenyl)-ethanone

https://huagongshe.com/reaction/274477

반응식

참여 물질

역할이름HCID투입량
반응물Boron tribromideHCID 25134—
반응물2-Bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenoneHCID 14450983—
용매DichloromethaneHCID 6344—
생성물2-Bromo-1-(3,4-dihydroxy-5-nitro-phenyl)-ethanoneHCID 21845596—

반응 단계

A suspension of 29.0 g of 2-bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenone in 700 ml of dry methylene chloride is treated at -20° within 30 minutes with a solution of 125.3 g of boron tribromide in 300 ml of dry methylene chloride. After the addition the mixture is stirred at -20° for a further 1 hour and at room temperature for 16 hours, then evaporated, the residue is treated cautiously with water while cooling with ice and stirred at 50° for 30 minutes. After cooling the mixture is extracted with ether, the ethereal phase is washed with water, dried over sodium sulfate, filtered and evaporated. There is obtained 2-bromo-3',4'-dihydroxy-5'-nitroacetophenone of m.p. 138°-140° (from methylene chloride).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05389653
출처 데이터셋uspto-grants-1995_02
ORD IDord-41984e31f2db426abf9494899f940258
출처 메모uspto-grants-1995_02