돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22131생성일: 2026년 10월 23일

Triethylamine → 6-(4-(2-(2,4,6-Trimethylbenzenesulphonylamino)ethyl)phenyl)-6-(3-pyridyl)hex-5-enoic acid

https://huagongshe.com/ko/reaction/22131

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Mesitylenesulfonyl chlorideHCID 13046—
반응물Methyl 6-(4-(2-aminoethyl)phenyl)-6-(3-pyridyl)hex-5-enoateHCID 54161160—
용매DichloromethaneHCID 6344—
생성물6-(4-(2-(2,4,6-Trimethylbenzenesulphonylamino)ethyl)phenyl)-6-(3-pyridyl)hex-5-enoic acidHCID 54316826—

반응 단계

A mixture of 3.24 g of methyl 6-(4-(2-aminoethyl)phenyl)-6-(3-pyridyl)hex-5-enoate, 2.2 g of 2,4,6-trimethylbenzenesulphonic acid chloride and 100 ml of triethylamine in 50 ml of dichloromethane is stirred for 30 minutes at ambient temperature. Then the reaction mixture is washed twice with water, dried and evaporated down. The residue is purified over a silica gel column using ethyl acetate. The crude product obtain is heated in a mixture of 32 ml of ethanol and 5 ml of 4N sodium hydroxide solution for 30 minutes to 50° to 60° C. The reaction mixture is evaporated down, the residue is taken up in 50 ml of water and washed with ethyl acetate. The aqueous phase is adjusted to pH 5 by the addition of citric acid and extracted twice with ethyl acetate. The organic phase is dried, evaporated down and the residue is chromatographed over a silica gel column using ethyl acetate. The crude product is then recrystallised from ethyl acetate/diisopropyl ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05426119
출처 데이터셋uspto-grants-1995_06
ORD IDord-7df537ef2af54ad2b761aab6a318ec77
출처 메모uspto-grants-1995_06