참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 2,2-Diphenylacetyl chloride | HCID 74637 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | Tri-n-butyl-((3,5-bis(trifluoromethyl)phenyl)methyloxymethyl)tin | HCID 85682165 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 1,1-Diphenylacetone | HCID 69907 | — |
반응 단계
Diphenylacetyl chloride (4.6 g), tri-n-butyl-((3,5-bis(trifluoromethyl)phenyl)methyloxymethyl)tin (12.6 g; Example 1a, (Method Ai)and benzylchlorobis(triphenylphosphine) palladium (II)(80 mg)were dissolved in chloroform (10 ml) and the solution heated at 80° C. for 6h. On cooling diethyl ether and saturated aqueous potassium fluoride were added and after 30 minutes the solution was filtered through Hiflo™. The organic layer was washed with water, saturated brine and dried (MgSO4). After evaporation in vacuo the residual oil was purified by chromatography on silica gel (eluting with 0 to 10% ethyl acetate in petroleum ether bp=60°-80° C.) to give 1-(3,5-bis(trifluoromethyl)phenyl)methyloxy)-3,3-diphenyl acetone as an oil. 1H NMR (CDCl3, 360MHz) δ7.80 (1H; s; 4-aryl CH) 7.71 (2H; s; 2,6-aryl CH), 7.43-7.24 (10H; m; phenyl), 5.30 (1H; s; Ph2CH), 4.56 (2H; s), 4.31 (2H; s). m/e Found 452.1191, C24H13F6O2 requires 452.12110.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05563161 |
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| 출처 데이터셋 | uspto-grants-1996_10 |
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| ORD ID | ord-cfa0d90d320c4607a1d2e6bcdc8c5fd8 |
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| 출처 메모 | uspto-grants-1996_10 |
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