돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31352생성일: 2026년 10월 23일

2-Bromoanisole → 3-Hydroxy-3-(2-methoxyphenyl)-5-trifluoromethoxy-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/ko/reaction/31352

반응식

참여 물질

역할이름HCID투입량
반응물2-BromoanisoleHCID 11358—
반응물Ammonium ChlorideHCID 25517—
반응물5-(trifluoromethoxy)-2,3-dihydro-1H-indole-2,3-dioneHCID 2732752—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3-Hydroxy-3-(2-methoxyphenyl)-5-trifluoromethoxy-1,3-dihydro-2H-indol-2-oneHCID 2190589976.3%
생성물HCID 178489560HCID 178489560—

반응 단계

A solution of 2-methoxyphenylmagnesium bromide is prepared starting with 1.9 g of magnesium in 4 ml of ether and a solution of 14.54 g of 1-bromo-2-methoxybenzene in 21 ml of ether. This solution is added dropwise, under an argon atmosphere, to a mixture of 5 g of 5-trifluoromethoxy-1H-indole-2,3-dione in 26 ml of THF, precooled on an ice bath, the resulting mixture is then heated at the reflux temperature of the ether for 1 hour 30 minutes and is allowed to cool to RT. The reaction mixture is poured slowly into saturated NH4Cl solution and extracted with EtOAc, the organic phase is washed with 5% K2CO3 solution, with water and with saturated NaCl solution and dried over Na2SO4, and the solvent is evaporated off under vacuum. 2.8 g of the expected product are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425566B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-c0c9fcda8b5943aea3d4da63af3bb7f5
출처 메모uspto-grants-2008_09