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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6087생성일: 2026년 10월 23일

Triethylamine → 1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine

https://huagongshe.com/ko/reaction/6087

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
용매DichloromethaneHCID 6344—
생성물1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 418486998.7%

반응 단계

To a solution of 1.00 g (4.97 mmol) of N-t-butoxycarbonyl-4-hydroxypiperidine and 0.83 ml (5.96 mmol) of triethylamine in 50 ml of methylene chloride was added 0.46 ml (5.96 mmol) of methanesulfonylchloride under ice-cooling and stirring and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with an aqueous saturated sodium bicarbonate solution and water and dried. The solvent was distilled off. The residue was washed with hexane to obtain 1.37 g of the desired compound (98.6%, colorless powder), mp: 87.0°-88.0° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246948
출처 데이터셋uspto-grants-1993_09
ORD IDord-7030c1fd7e86451f857a9e61a4bc804b
출처 메모uspto-grants-1993_09