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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1672381생성일: 2026년 10월 27일

Dimethyl Sulfoxide → 1-(((Tert-butyldimethylsilyl)oxy)methyl)cyclopropane-1-carbaldehyde

https://huagongshe.com/reaction/1672381

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물(1-(((tert-Butyldimethylsilyl)oxy)methyl)cyclopropyl)methanolHCID 59000904—
용매DichloromethaneHCID 6344—
생성물1-(((Tert-butyldimethylsilyl)oxy)methyl)cyclopropane-1-carbaldehydeHCID 8661456266%

반응 조건

온도-70 °C

반응 단계

To a stirred solution of DMSO (6.9 mL, 0.097 mol) in anhydrous DCM (90 mL) at −70° C. was added oxalyl chloride (4.20 mL, 0.0486 mol). After stirring for 10 min. at −70° C., a solution of [1-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclopropyl]methanol (7.011 g, 0.03240 mol) in anhydrous DCM (30 mL) was added via cannula. The resulting milky mixture was slowly warmed to −55° C. over 45 min. DIPEA (34.0 mL, 0.194 mol) was added. The resulting mixture was stirred for 5 min. at −55° C., and then the cooling bath was removed and the reaction mixture was allowed to warm to RT. The reaction was then quenched with saturated aqueous NaHCO3 (150 mL) and extracted with DCM (2×). The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The resulting residue was purified by Combiflash chromatography eluting with 0-10% EtOAc/hexanes to afford the desired product as a colorless oil (4.558 g, 66% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07998959B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-a31dd94b3304489db4db2711a03299fd
출처 메모uspto-grants-2011_08