Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1662176생성일: 2026년 10월 27일
Methanol → N-((3-Bromo-4-fluorophenyl)(2-cyano-3-fluorophenyl)methylene)-2-methylpropane-2-sulfinamide
https://huagongshe.com/reaction/1662176
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Tert-Butanesulfinamide | HCID 3382465 | — |
| 반응물 | 2-(3-Bromo-4-fluoro-benzoyl)-6-fluoro-benzonitrile | HCID 58579483 | — |
| 촉매 | Titanium tetraethoxide | HCID 76524 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-((3-Bromo-4-fluorophenyl)(2-cyano-3-fluorophenyl)methylene)-2-methylpropane-2-sulfinamide | HCID 76821603 | 55% |
반응 단계
2-(3-Bromo-4-fluoro-benzoyl)-6-fluoro-benzonitrile (7.9 g, 24.5 mmol) dissolved in dry THF (40 mL) was added to a solution of titanium (IV) ethoxide (12.7 ml, 61.3 mmol) in dry THF (30 mL) at room temperature. 2-Methyl-2-propanesulfinamide (3.57 g, 29.4 mmol) was added and the resulting mixture was heated at reflux temperature for 22 h. The reaction mixture was cooled to room temperature and methanol (120 mL) was added, followed by addition of saturated sodium bicarbonate (12 mL). The resulting suspension was filtered through a pad of sodium sulfate and the solids were washed thoroughly with ethyl acetate. The filtrate was concentrated in vacuo and purified by flash column chromatography using a gradient of 30-50% ethyl acetate in hexanes to afford 5.7 g (55% yield) of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08030500B2 |
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| 출처 데이터셋 | uspto-grants-2011_10 |
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| ORD ID | ord-b48e773ef98e438fa28a94f8d8d8d14d |
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| 출처 메모 | uspto-grants-2011_10 |
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