Chloral → 1,1,1-Trichloro-5-ethyl-2-hydroxy-5-methylheptan-4-one
反応式
[C:1]([C:4]([CH2:8][CH3:9])([CH3:7])[CH2:5][CH3:6])(=[O:3])[CH3:2].[O:10]=[CH:11][C:12]([Cl:15])([Cl:14])[Cl:13]>C(O)(=O)C>[Cl:13][C:12]([Cl:15])([Cl:14])[CH:11]([OH:10])[CH2:2][C:1](=[O:3])[C:4]([CH2:8][CH3:9])([CH3:7])[CH2:5][CH3:6]参加物
4
実験手順
A 30 g. portion of the product of Preparation 2, 1-acetyl-1-ethyl-1-methylpropane, was combined with 38.4 g. of chloral and 36 ml. of acetic acid, and was stirred under reflux, under nitrogen, for 4 days. The solvent was then carefully removed under vacuum to obtain 39 g. of the crude product as an amber, viscous oil.
後処理
- temperatureunder reflux, under nitrogen, for 4 days
- customThe solvent was then carefully removed under vacuum
- customto obtain 39 g
出典と根拠
- ORDレコード
- ord-1be3a4899acd480f915000e78359c592
- 出典データセット
- uspto-grants-1983_10
- 特許番号
- US04411753
反応ノート
読み込み中…