Water → Ethanone, 2-hydroxy-2-phenyl-1-(3-pyridinyl)-
反応式
Br.Br[CH:3]([C:10]([C:12]1[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=1)=[O:11])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.C([O-])(=[O:20])C.[K+].O>C(OC(=O)C)(=O)C>[OH:20][CH:3]([C:10]([C:12]1[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=1)=[O:11])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1参加物
実験手順
Alternatively, a mixture of 20.0 g (56.0 mmoles) of 3-pyridyl α-bromobenzyl ketone hydrobromide and 24.0 g (0.24 mole) of potassium acetate in 100 ml of acetic anhydride was stirred overnight at room temperature. The reaction mixture was poured into water and the product extracted into ether. The combined ether layers were washed with water and then 10% aqueous sodium bicarbonate solution. The ether layer was dried over potassium carbonate and evaporated. A solution of the residue in 140 ml of 1 N aqueous hydrochloric acid was heated at reflux for 30 minutes and after cooling made basic with solid sodium carbonate. The product was extracted into ether and the combined ether extracts evaporated, after drying over anhydrous potassium carbonate, to give 8.15 g of 3-pyridyl α-hydroxybenzyl ketone.
後処理
- extractionthe product extracted into ether
- washThe combined ether layers were washed with water
- dry with materialThe ether layer was dried over potassium carbonate
- customevaporated
- temperatureA solution of the residue in 140 ml of 1 N aqueous hydrochloric acid was heated
- temperatureat reflux for 30 minutes
- temperatureafter cooling
- extractionThe product was extracted into ether
- customthe combined ether extracts evaporated
- dry with materialafter drying over anhydrous potassium carbonate
出典と根拠
- ORDレコード
- ord-1ccac70cca1c495e93f97daeeddfa1a3
- 出典データセット
- uspto-grants-1979_06
- 特許番号
- US04159338
反応ノート
読み込み中…