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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483406생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/483406

반응식

참여 물질

역할이름HCID투입량
반응물Benzal chlorideHCID 7411—
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 5-chloro-3-thiophenylindole-2-carboxylateHCID 67902874—
반응물Potassium hexamethylsilamideHCID 131717145—
촉매Tetrabutylammonium BromideHCID 74236—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매HexamethylphosphoramideHCID 12679—
생성물Ethyl 1-(p-chlorobenzyl)-5-chloro-3-thiophenylindole-2-carboxylateHCID 67855865—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05225421
출처 데이터셋uspto-grants-1993_07
ORD IDord-c149c78e537a4b2aaf0a44152e4574ab
출처 메모uspto-grants-1993_07