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Acetone → 7-fluoro-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetone | HCID 180 | — |
| 反応物 | Pyrrolidine | HCID 31268 | — |
| 反応物 | 4'-Fluoro-2'-hydroxyacetophenone | HCID 2737326 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 7-fluoro-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one | HCID 15205373 | 53% |
反応手順
1-(4-Fluoro-2-hydroxy-phenyl)-ethanone (5.0 g, 32.44 mmol), acetone (11.92 mL, 162.2 mmol) and pyrrolidine (2.7 mL, 32.44 mmol) were dissolved in 20 mL benzene, and the reaction mixture was refluxed for four hours. The reaction mixture was cooled to room temperature and partitioned between ethyl acetate and 1 N HCl. The organic layer was dried over MgSO4, and solvent was evaporated under reduced pressure. The resulting residue was chromatographed (15% ethyl acetate in hexanes eluting through silica) and solvent was removed to yield 3.33 g (17.16 mg, 53%) of 7-fluoro-2,2-dimethyl-chroman-4-one as an oil. MS: 195 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07528250B2 |
| 出典データセット | uspto-grants-2009_05 |
| ORD ID | ord-4df5a3bcc2434497a2a7b54276b5a6ba |
| 出典メモ | uspto-grants-2009_05 |