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HRID 1829047생성일: 2026년 10월 26일

Hydrochloric Acid → 3-(5-Bromo-2-benzofuran-1(3H)-ylidene)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1829047

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물OxindoleHCID 321710—
반응물5-BromophthalideHCID 603144—
반응물LiHMDS tetrahydrofuranHCID 23714775—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매1,2-DimethoxyethaneHCID 8071—
생성물3-(5-Bromo-2-benzofuran-1(3H)-ylidene)-1,3-dihydro-2H-indol-2-oneHCID 6965924277.2%

반응 단계

To a stirred solution of oxindole (3.13 g, 23.5 mmol) in anhydrous dimethoxyethane (20 ml) under nitrogen was added 1.0M LiHMDS/THF solution (49 ml, 49 mmol). The mixture was stirred at room temperature for 10 minutes, and 5-bromophthalide (3.00 g, 14.1 mmol) was added. The reaction mixture was stirred at room temperature for 3 hours and then poured into a mixture of THF (50 ml) and 2M HCl aqueous solution (50 ml). After heated at reflux for 1 hour and then cooled to room temperature, the resulting mixture was poured into water (100 ml). The resulting solid was filtered, washed with water and dried under vacuum to give 3-(5-bromo-3H-isobenzofuran-1-ylidene)-1,3-dihydro-indol-2-one as a yellow solid (3.57 g, 77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07060844B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-fd1637c97421450eac1d5663cb8762fa
출처 메모uspto-grants-2006_06