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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72201생성일: 2026년 10월 24일

Pyridine → Tert-butyl (3R)-3-(methanesulfonyloxy)pyrrolidine-1-carboxylate

https://huagongshe.com/ko/reaction/72201

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Ethyl AcetateHCID 8857—
반응물Methanesulfonyl chlorideHCID 31297—
반응물tert-Butyl (3S)-3-hydroxypyrrolidine-1-carboxylateHCID 854055—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Tert-butyl (3R)-3-(methanesulfonyloxy)pyrrolidine-1-carboxylateHCID 10934372—

반응 조건

온도50 °C

반응 단계

Methanesulfonyl chloride was added to a mixture of (S)-3-hydroxypyrrolidine-1-carboxylic acid tert-butyl ester (40 g) and pyridine (17.4 g) in dichloromethane (400 mL) at 0° C. The reaction mixture was stirred at this temperature for 15 min and then heated at 50° C. for 8 h. The reaction mixture was subsequently mixed with ethyl acetate and water, and the ethyl acetate phase was washed with dil. HCl solution. The ethyl acetate phase was dried over sodium sulfate and the solvent was removed in vacuo. The (R)-3-methanesulfonyloxypyrrolidine-1-carboxylic acid tert-butyl ester obtained in this way was dissolved in pyrrolidine (18.2 mL), and the reaction mixture was heated to 100° C. The reaction mixture was then mixed with ethyl acetate and water. The ethyl acetate phase was washed several times with water. The organic phase was dried over sodium sulfate and the solvent was removed in vacuo.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828991B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-727bc034e03f46d881500135dc23264a
출처 메모uspto-grants-2014_09