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HRID 20011생성일: 2026년 10월 25일

Triethylsilanol → (NE,R)-N-[2-[1-[tert-butyl(dimethyl)silyl]oxycyclopropyl]ethylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/20011

반응식

참여 물질

역할이름HCID투입량
반응물TriethylsilanolHCID 69005—
반응물tert-Butylsulfinamide, (R)-(+)-HCID 10964479—
반응물2-{1-[(Tert-butyldimethylsilyl)oxy]cyclopropyl}acetaldehydeHCID 86614119—
용매DichloromethaneHCID 6344—
생성물(NE,R)-N-[2-[1-[tert-butyl(dimethyl)silyl]oxycyclopropyl]ethylidene]-2-methylpropane-2-sulfinamideHCID 87349123—

반응 조건

온도23 °C

반응 단계

To a 1.0 L round bottom flask containing 2-(1-(tert-butyldimethylsilyloxy)cyclopropyl)acetaldehyde (5.00 g, 23.3 mmol) (crude 10.5 g with TESOH, 1H NMR showed about 50/50 sm to impurity) was added DCM (200 mL) and the mixture was allowed to stir at 23° C. for 5 min. At this time, (R)-2-methylpropane-2-sulfinamide (2.83 g, 23.3 mmol) and cupric sulfate anhydrous (2.58 ml, 58.3 mmol) were added and the reaction was allowed to stir for 40 h. The copper salts were removed by celite filtration. The filtrate was concentrated to give a yellow oil that was purified on a 330 g Isco column (5 to 20% EtOAc in hexanes)to afford the title compound as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745484B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-97b820d84b6847df95d2262091e04ca6
출처 메모uspto-grants-2010_06