돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54544생성일: 2026년 10월 24일

Triethylamine → tert-Butyl 4-(2-((methanesulfonyl)oxy)ethyl)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/54544

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 854140—
용매DichloromethaneHCID 6344—
생성물tert-Butyl 4-(2-((methanesulfonyl)oxy)ethyl)piperidine-1-carboxylateHCID 15229596—

반응 단계

A solution of methanesulfonyl chloride (0.51 ml) in methylene chloride (5 ml) was added dropwise to a mixture of 4-(2-hydroxyethyl)-1-tert-butoxycarbonylpiperidine (1.43 g) and triethylamine (0.91 ml) at 5° C. After stirring at ambient temperature for 1 hour, the mixture was poured into ice water and extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo to give 1-tert-butoxycarbonyl-4-(2-mesyloxyethyl)piperidine (1.37 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622976
출처 데이터셋uspto-grants-1997_04
ORD IDord-5cfeb3dd818c45089f6ebdb5dc7bffac
출처 메모uspto-grants-1997_04