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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1518457생성일: 2026년 10월 26일

Triethylamine → Benzyl 4-((methanesulfonyl)oxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1518457

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Benzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
용매DichloromethaneHCID 6344—
생성물Benzyl 4-((methanesulfonyl)oxy)piperidine-1-carboxylateHCID 58303455101.3%

반응 단계

To a stirring solution of benzyl 4-hydroxy-1-piperidinecarboxylate (3.55 mL, 23.4 mmol, Aldrich) and Et3N (7.18 mL, 51.5 mmol, Aldrich) in CH2Cl2 (25 mL) at room temperature was added a solution of methanesulfonyl chloride (1.99 mL, 25.8 mmol, Acros) in CH2Cl2 (25 mL) dropwise. The reaction mixture was stirred at room temperature for 1 h and washed with 1N HCl aqueous solution, H2O and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to yield 7.43 g of the desired product as a yellow oil. MS (ESI) 314 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08232404B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-274433c472cf456ebca9ec8143882b98
출처 메모uspto-grants-2012_07