Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57461생성일: 2026년 10월 23일
tert-Butylsulfinamide, (R)-(+)- → (NE,R)-N-[[4-(1,1-difluoroethyl)-2-fluorophenyl]methylidene]-2-methylpropane-2-sulfinamide
https://huagongshe.com/ko/reaction/57461
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-Butylsulfinamide, (R)-(+)- | HCID 10964479 | — |
| 반응물 | 4-(1,1-Difluoroethyl)-2-fluorobenzaldehyde | HCID 90414785 | — |
| 촉매 | Copper Sulfate | HCID 24462 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | (NE,R)-N-[[4-(1,1-difluoroethyl)-2-fluorophenyl]methylidene]-2-methylpropane-2-sulfinamide | HCID 90414196 | 46.3% |
반응 단계
To a mixture of 4-(1,1-difluoroethyl)-2-fluorobenzaldehyde (693 mg, from Step 4) and (R)-2-methylpropane-2-sulfinamide (513 mg, 4.24 mmol) in DCE (12.9 mL) was added copper(II) sulfate (882 mg, 5.52 mmol). The reaction mixture was placed in a pre-heated oil bath (55° C.) and heated for ˜2 d. The mixture was allowed to cool to room temperature, filtered through a pad of celite and rinsed with DCE. The combined filtrates were concentrated under reduced pressure. The residue was purified by column chromatography [SiO2, 24 g, heptane/ethyl acetate] providing (R,E)-N-(4-(1,1-difluoroethyl)-2-fluorobenzylidene)-2-methylpropane-2-sulfinamide (497 mg) as a yellow oil. LCMS m/z 292.1 (M+H)+, Rt 0.97 min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434719B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-574f6ecd80b143f8b47b401ea8b0dd74 |
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| 출처 메모 | uspto-grants-2016_09 |
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