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HRID 1829047作成日:2026年10月27日

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

https://huagongshe.com/reaction/1829047

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物OxindoleHCID 321710—
反応物5-BromophthalideHCID 603144—
反応物LiHMDS tetrahydrofuranHCID 23714775—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物3-(5-Bromo-2-benzofuran-1(3H)-ylidene)-1,3-dihydro-2H-indol-2-oneHCID 6965924277.2%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07060844B2
出典データセットuspto-grants-2006_06
ORD IDord-fd1637c97421450eac1d5663cb8762fa
出典メモuspto-grants-2006_06