Acetone → 1-(6-methyl-3,4-dihydro-2H-pyran-5-yl)ethan-1-one
反応式
[CH3:1][C:2](=[O:7])[CH2:3][C:4](=[O:6])[CH3:5].C(=O)([O-])[O-].[K+].[K+].[I-].[Na+].[CH3:16][C:17]([CH3:19])=O>>[C:4]([C:3]1[CH2:16][CH2:17][CH2:19][O:7][C:2]=1[CH3:1])(=[O:6])[CH3:5]参加物
5
実験手順
A mixture of 130.4 g. (1.3 moles) of 2,4-pentanedione, 251.9 g. (1.6 moles) of 1,3-bromochloropropane, 168 g. (1.2 moles) of anhydrous potassium carbonate, 1 g. of anhydrous sodium iodide and 250 ml. of dry acetone is refluxed for 20 hours, under exclusion of humidity, with stirring. After cooling the mixture is filtered, washed with four 150-ml. portions of dry acetone, the combined acetone extract is evaporated, and the residue is subjected to fractionated distillation in vacuum, on a Vigreux column.
後処理
- additionA mixture of 130.4 g
- temperatureAfter cooling the mixture
- filtrationis filtered
- washwashed with four 150-ml
- extractionportions of dry acetone, the combined acetone extract
- customis evaporated
- distillationthe residue is subjected to fractionated distillation in vacuum, on a Vigreux column
出典と根拠
- ORDレコード
- ord-0cbee646f764447887e4926ad61faec7
- 出典データセット
- uspto-grants-1989_06
- 特許番号
- US04843080
反応ノート
読み込み中…