Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57423생성일: 2026년 10월 23일
2-Fluoro-4-(trifluoromethyl)benzaldehyde → (NE,R)-N-[[2-fluoro-4-(trifluoromethyl)phenyl]methylidene]-2-methylpropane-2-sulfinamide
https://huagongshe.com/ko/reaction/57423
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Fluoro-4-(trifluoromethyl)benzaldehyde | HCID 522929 | — |
| 반응물 | tert-Butylsulfinamide, (R)-(+)- | HCID 10964479 | — |
| 촉매 | Copper Sulfate | HCID 24462 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | (NE,R)-N-[[2-fluoro-4-(trifluoromethyl)phenyl]methylidene]-2-methylpropane-2-sulfinamide | HCID 89479418 | 95% |
반응 단계
To a oven dried round bottom flask with stir bar was added 2-fluoro-4-(trifluoromethyl)benzaldehyde (5 g, 26.0 mmol), (R)-2-methylpropane-2-sulfinamide (3.47 g, 28.6 mmol) and DCE (52 mL). To this mixture was then added copper (II) sulfate (6.23 g, 39.0 mmol). The reaction mixture was heated in a preheated oil bath at 55° C. for 18 hours. The reaction mixture was filtered through a pad celite, washing the solids with DCE. The filtrate was concentrated to afford a viscous green oil of (R,E)-N-(2-fluoro-4-(trifluoromethyl)benzylidene)-2-methyl propane-2-sulfinamide (7.3 g, 24.7 mmol, 95% yield). Material was taken onto next step without further purification. 1H NMR (400 MHz, CDCl3) δ ppm 1.29 (s, 9H) 7.44 (d, J=10.08 Hz, 1H) 7.51 (d, J=8.27 Hz, 1H) 8.13 (t, J=7.46 Hz, 1H) 8.92 (s, 1H). LCMS m/z 296.0 (M+H)+, Rt 1.02 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-59cb2e214ed8410eb0426c4a8765abe5 |
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| 출처 메모 | uspto-grants-2016_09 |
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