참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 4-bromo-N,N-dimethylaniline | HCID 11465 | — |
| 반응물 | alpha,alpha-Difluorophenylacetate | HCID 6928296 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 용매 | Pentane | HCID 8003 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2,2-Difluoro-1-[4-(dimethylamino)phenyl]-2-phenylethanone | HCID 15728459 | 31.8% |
반응 단계
A solution of 4.0 g of 4-bromo-N,N-dimethylaniline in 50 ml of dry tetrahydrofuran at -78° C. was treated with 23.5 ml of 1.7M tert-butyllithium in pentane under nitrogen over 5 minutes with rapid stirring. After 0.5 hour, the slurry was warmed to -30° C. and added to a solution of 4.0 g of α,α-difluorophenylacetate in 50 ml of dry tetrahydrofuran at -78° C. After 1 hour at -78° C., the solution was allowed to warm to room temperature and stirred overnight. The solution was poured into water and extracted with ethyl acetate. Evaporation left a solid which was purified by flash chromatography (1:1 ethyl acetate-hexane) to give a powder. Recrystallization from ethyl acetate-hexane gave 1.75 g of 2,2-difluoro-1-[4-(dimethylamino)phenyl]-2-phenylethanone, m.p. 115°-116° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05006563 |
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| 출처 데이터셋 | uspto-grants-1991_04 |
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| ORD ID | ord-3e5a35d81762490084a0d076b55aaf7b |
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| 출처 메모 | uspto-grants-1991_04 |
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