Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 2-[4-(Trifluoromethyl)phenyl]oxirane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Trimethylsulfonium iodide | HCID 75127 | — |
| 반응물 | 1-Ethenyl-4-(trifluoromethyl)benzene | HCID 2782798 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | 2-[4-(Trifluoromethyl)phenyl]oxirane | HCID 9990016 | 81% |
반응 단계
Trimethylsulfonium iodide (4.08 g, 20.0 mmol) in dimethyl sulfoxide (15 mL) was stirred with sodium hydride (55 wt % dispersion in mineral oil, 873 mg, 20.0 mmol) at room temperature for 1 hour and then with 4-(trifluoromethyl)styrene (2.96 g, 17.0 mmol) in dimethyl sulfoxide (10 mL) at room temperature for 2 hours. After addition of water, the reaction mixture was extracted with ethyl acetate, and the organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=9/1 (v/v)) to give the title compound as a colorless oil (2.59 g, yield 81%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09216999B2 |
| 출처 데이터셋 | uspto-grants-2015_12 |
| ORD ID | ord-f886d7f436004bc58563b288f1ce0f26 |
| 출처 메모 | uspto-grants-2015_12 |