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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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물1-(tert-Butyldimethylsilyloxy)-2-propanoneHCID 4124969—
반응물tert-Butylsulfinamide, (S)-(-)-HCID 11355477—
촉매Titanium(IV)ethoxideHCID 2724286—
용매TetrahydrofuranHCID 8028—
생성물(NE,S)-N-[1-[tert-butyl(dimethyl)silyl]oxypropan-2-ylidene]-2-methylpropane-2-sulfinamideHCID 90089971—

반응 조건

온도70 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09278968B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-81a2ccdcebbb4547ac546954f461f188
출처 메모uspto-grants-2016_03