참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Acetyl-4-fluorophenol | HCID 95992 | — |
| 반응물 | Glycidyl tosylate, (R)- | HCID 154187 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 5-Fluoro-2-((R)-1-(oxiranylmethoxy)-phenyl]-ethanone | HCID 86644723 | 76% |
반응 단계
A mixture of 5′-fluoro-2′-hydroxyacetophenone (2.04 g, 13.25 mmol), (2R)-(−)-glycidyl tosylate (2.75 g, 12.05 mmol), potassium carbonate (2.16 g, 15.66 mmol) and N,N-dimethyl formamide (20 ml) was heated to 60° C. After 6 hours the reaction mixture was cooled down, water (20 ml) and ethyl acetate (20 ml) were added and the layers were separated. Organic phase was recovered and water layer was extracted twice with ethyl acetate. Organic phase and ethyl acetate extracts were combined and washed twice with water and evaporated to dryness. The crude product was crystallized from 2-propanol to yield 1.91 g (76%) of the pure title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08492549B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-c7d4a2358b2f49a28f5e53ad7b6b46e1 |
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| 출처 메모 | uspto-grants-2013_07 |
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