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HRID 1090265作成日:2026年10月27日

1-Chloro-4-(chloromethyl)benzene → Ethyl 1-(p-chlorobenzyl)-5-chloro-3-thiophenylindole-2-carboxylate

https://huagongshe.com/reaction/1090265

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloro-4-(chloromethyl)benzeneHCID 7723—
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 0.62M 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 p-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US05081138
出典データセットuspto-grants-1992_01
ORD IDord-d7aaa2792f3c4a489604a471a7db3a0a
出典メモuspto-grants-1992_01