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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219762생성일: 2026년 10월 26일

Water → 3-Hydroxy-4,6-dichloro-1,3-dihydro-3-(4-trifluoromethylphenyl)indol-2-one

https://huagongshe.com/reaction/219762

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
반응물4,6-DichloroisatinHCID 251908—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3-Hydroxy-4,6-dichloro-1,3-dihydro-3-(4-trifluoromethylphenyl)indol-2-oneHCID 66602670—

반응 단계

1.8 g of Grignard magnesium are placed in 19 ml of anhydrous ethyl ether in a round-bottomed flask equipped with a mechanical stirrer, and under a stream of nitrogen. A mixture of 8.9 ml of 4-bromotrifluoromethylbenzene in 46 ml of anhydrous ethyl ether is then added. The mixture is stirred for one hour, followed by addition of a solution of 5.7 g of 4,6-dichloro-1H-indole-2,3-dione in 100 ml of anhydrous THF. The mixture is stirred at room temperature for 4 hours 30 minutes. Water is added and the resulting mixture is extracted with ethyl acetate. The organic phase is separated out and dried over Na2SO4, filtered and evaporated under vacuum. The residue is taken up in ethyl acetate and washed with 1N sodium hydroxide solution. The organic phase is dried over Na2SO4, filtered and evaporated under vacuum. The solid is taken up in ethyl ether and filtered off. 4.7 g of expected product are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202871B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-15e2988c599d4d829b0be32d5a2db277
출처 메모uspto-grants-2012_06