Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylsilanol | HCID 69005 | — |
| 반응물 | tert-Butylsulfinamide, (R)-(+)- | HCID 10964479 | — |
| 반응물 | 2-{1-[(Tert-butyldimethylsilyl)oxy]cyclopropyl}acetaldehyde | HCID 86614119 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (NE,R)-N-[2-[1-[tert-butyl(dimethyl)silyl]oxycyclopropyl]ethylidene]-2-methylpropane-2-sulfinamide | HCID 87349123 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07745484B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-97b820d84b6847df95d2262091e04ca6 |
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| 출처 메모 | uspto-grants-2010_06 |
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