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Isopropanol → 1-Chloro-3-(4-fluorophenyl)hex-5-en-3-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isopropanol | HCID 3776 | — |
| 反応物 | Binol | HCID 11762 | — |
| 反応物 | 2-Chloro-4'-fluoropropiophenone | HCID 67672 | — |
| 反応物 | Tetrallylstannane | HCID 81878 | — |
| 触媒 | Titanium isopropoxide | HCID 11026 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-Chloro-3-(4-fluorophenyl)hex-5-en-3-ol | HCID 53472938 | — |
反応手順
To a solution of 1,1′-bi-2-naphthol (0.2280 g, 0.80 mmol, 0.26 equiv), CH2Cl2 (5 mL) and titanium(IV) isopropoxide (0.2243 g, 0.79 mmol, 0.26 equiv) were added 2-propanol (3.1620 g, 52.6 mmol, 17 equiv), tetraallylstannane (1.2538 g, 4.43 mmol, 1.43 equiv), and 3-chloro-1-(4-fluorophenyl)propan-1-one (0.5760 g, 3.09 mmol, 1.0 equiv) successively. The reaction mixture was stirred at rt under nitrogen for 22 h. The reaction was quenched with satd aq NH4Cl and extracted with EtOAc. The organic layer was dried over Na2SO4. After the solvents were evaporated, the residue was purified by chromatography on silica gel eluted with hexanes/ethyl acetate to afford 1-chloro-3-(4-fluorophenyl)hex-5-en-3-ol as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08487094B2 |
| 出典データセット | uspto-grants-2013_07 |
| ORD ID | ord-f38ad47adc164f30938f3185cfebd733 |
| 出典メモ | uspto-grants-2013_07 |