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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49970생성일: 2026년 10월 24일

Methanesulfonyl chloride → 1-tert-Butyl 2-methyl (2S,4R)-4-((methanesulfonyl)oxy)pyrrolidine-1,2-dicarboxylate

https://huagongshe.com/ko/reaction/49970

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물(2S,4R)-4-Hydroxypyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl esterHCID 2734883—
용매DichloromethaneHCID 6344—
생성물1-tert-Butyl 2-methyl (2S,4R)-4-((methanesulfonyl)oxy)pyrrolidine-1,2-dicarboxylateHCID 14772682—

반응 조건

온도20 °C

반응 단계

To a solution of trans-N-Boc-4-hydroxy proline methyl ester (17.6 g) (0.072 mol) and TEA (12.5 mL) (0.09 mol) in 100 mL of DCM at 0° C. was slowly added methanesulfonyl chloride (7 mL) (0.09 mol). The temperature was allowed to warm to 20° C., and the mixture was stirred overnight. Insoluble material was removed by filtration and the organic layer washed with water, dried over MgSO4, and evaporated in vacuo to afford the above-titled compound as an oil which solidified upon standing (24 g). NMR(CDCl3, 200 MHz): 5.22 (1H, m), 4.32-4.5 (1H, m), 3.5-3.9 (5H, m), 3.05 (3H, s), 2.5-2.73 (1H, m), 2.15-2.35 (1H, m), 1.35-1.5 (9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710064B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-66ebfcfad78b497c97691701722679dc
출처 메모uspto-grants-2004_03