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HRID 483406作成日:2026年10月26日

Benzal chloride → Ethyl 1-(p-chlorobenzyl)-5-chloro-3-thiophenylindole-2-carboxylate

https://huagongshe.com/reaction/483406

反応式

関与物質

役割名称HCID仕込み量
反応物Benzal chlorideHCID 7411—
反応物Ammonium ChlorideHCID 25517—
反応物Ethyl 5-chloro-3-thiophenylindole-2-carboxylateHCID 67902874—
反応物Potassium hexamethylsilamideHCID 131717145—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒HexamethylphosphoramideHCID 12679—
生成物Ethyl 1-(p-chlorobenzyl)-5-chloro-3-thiophenylindole-2-carboxylateHCID 67855865—

反応手順

To a cold (-78°), stirred solution containing 664 mg of ethyl 5-chloro-3-thiophenylindole-2-carboxylate from Preparation 5 in 3.5 mL of dry tetrahydrofuran, under argon, was added 3.5 mL of a 0.62 M solution of potassium hexamethylsilamide in toluene. The reaction mixture was stirred at -78° for 1 h and at 0° for 1 h then recooled to -78°. 0.75 mL of g chlorobenzyl chloride, 1.0 mL of hexamethylphosphoric triamide and 20 mg of tetra-n-butylammonium bromide were then added. The resultant mixture was allowed to warm to room temperature and stirred for 18 h. Saturated aqueous ammonium chloride and ether were added. The ether layer was separated, washed with water, 10% aqueous cupric sulfate, water and brine and dried over MgSO4.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05225421
出典データセットuspto-grants-1993_07
ORD IDord-c149c78e537a4b2aaf0a44152e4574ab
出典メモuspto-grants-1993_07