Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 923501생성일: 2026년 10월 26일
Sodium Chloride → (NE,S)-N-[1-[tert-butyl(dimethyl)silyl]oxypropan-2-ylidene]-2-methylpropane-2-sulfinamide
https://huagongshe.com/reaction/923501
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | 1-(tert-Butyldimethylsilyloxy)-2-propanone | HCID 4124969 | — |
| 반응물 | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| 촉매 | Titanium(IV)ethoxide | HCID 2724286 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (NE,S)-N-[1-[tert-butyl(dimethyl)silyl]oxypropan-2-ylidene]-2-methylpropane-2-sulfinamide | HCID 90089971 | — |
반응 단계
To a solution of 761 mg of 1-{[tert-butyl (dimethyl)silyl]oxy}acetone in 20 ml of THF were added 2.1 ml of tetraethyl orthotitanate and 490 mg of (S)-2-methylpropane-2-sulfinamide, followed by stirring at 70° C. for 8 hours. The reaction mixture was left to be cooled to room temperature and a saturated aqueous sodium chloride solution was then added thereto, followed by stirring and filtering over Celite. The filtrate was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was then evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain (S)—N-[(2E)-1-{[tert-butyl(dimethyl)silyl]oxy}propan-2-ylidene]-2-methylpropane-2-sulfinamide.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09278968B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-81a2ccdcebbb4547ac546954f461f188 |
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| 출처 메모 | uspto-grants-2016_03 |
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