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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1596003생성일: 2026년 10월 26일

Toluene → 1-{(2-Ethoxycarbonylvinyl)-[4-(4-fluorophenoxy) benzenesulfonyl]-amino}cyclopentanecarboxylic Acid Benzyl Ester

https://huagongshe.com/reaction/1596003

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Ethyl propiolateHCID 12182—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물1-[4-(4-Fluorophenoxy)benzenesulfonylamino]-cyclopentanecarboxylic acid benzyl esterHCID 11005171—
용매TetrahydrofuranHCID 8028—
생성물1-{(2-Ethoxycarbonylvinyl)-[4-(4-fluorophenoxy) benzenesulfonyl]-amino}cyclopentanecarboxylic Acid Benzyl EsterHCID 54391412—

반응 단계

A solution of 25.0 g (532 mmol) of 1-[4-(4-fluorophenoxy)benzenesulfonylamino]cyclopentane-carboxylic acid benzyl ester and 10.8 mL (106 mmol, 2 equivalents) of ethyl propiolate in 200 mL of dry tetrahydrofuran at 1° C. was treated with 53.2 mL (53.2 mmol, 1 equivalent) of a solution of tetrabutylammonium fluoride in tetrahydrofuran (1M) over 45 minutes. The resulting solution was allowed to warm slowly to ambient temperature and stirred overnight, The tetrahydrofuran was displaced with toluene at reduced pressure, and the toluene solution was washed with water and brine, diluted to 600 mL with toluene, stirred with 90 g of silica gel for three hours, filtered, and concentrated to 25.14 g (83%) of 1-{(2-ethoxycarbonyivinyl)-[4-(4-fluorophenoxy)benzenesulfonyl]amino}-cyclopentanecarboxylic acid benzyl ester as an orangea oil. 1H NMR (CDCl3) indicated a 1.5:1 translcis ratio.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06288246B1
출처 데이터셋uspto-grants-2001_09
ORD IDord-2ffc025b178644c6ab8f4ba02e541815
출처 메모uspto-grants-2001_09