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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 906437생성일: 2026년 10월 25일

Triethylamine → [1-({[tert-Butyl(dimethyl)silyl]oxy}methyl)cyclopropyl]methyl methanesulfonate

https://huagongshe.com/reaction/906437

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물(1-(((tert-Butyldimethylsilyl)oxy)methyl)cyclopropyl)methanolHCID 59000904—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물[1-({[tert-Butyl(dimethyl)silyl]oxy}methyl)cyclopropyl]methyl methanesulfonateHCID 59000927—

반응 조건

온도0 °C

반응 단계

A solution of [1-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclopropyl]methanol (Example 34c, 5.37 g) dissolved in DCM (20 mL) was treated with triethylamine (6.92 mL) at 0° C. before adding methanesulfonyl chloride (2.321 mL) under nitrogen. The resulting mixture was stirred at 0° C. for 30 min. The reaction mixture was diluted with water (100 mL), and extracted with DCM (250 mL). The organics were dried (MgSO4), filtered and evaporated. The crude product was purified (SiO2 chromatography, elution 50% isohexane in diethyl ether). Pure fractions were evaporated to dryness to afford the subtitle compound (5.37 g) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08012980B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-2be7449450db4b7bb51f95b6aae5ad43
출처 메모uspto-grants-2011_09