Hydrochloric Acid → 1-Phenyl-3-chloro-3-cyclohexylpropan-1-one
反応式
[C:1]1([C:7](=[O:17])[CH2:8][CH:9](O)[CH:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:18]>>[C:1]1([C:7](=[O:17])[CH2:8][CH:9]([Cl:18])[CH:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
3
実験手順
The reaction and post treatment were carried out in the same manner as in Example 10 except that 1-phenyl-3-hydroxy-3-cyclohexylpropan-1-one obtained by the same production process as in Preparation Example 1, was used as the starting material, and hydrochloric acid (180 g) was changed to hydrogen chloride gas (20° C., 12,300 ml, 511 mmol), and the reaction was carried out at −20° C., whereby the desired 1-phenyl-3-chloro-3-cyclohexylpropan-1-one (97.1 g, 407 mmol) was obtained in a yield of 96%.
後処理
- customThe reaction and post treatment
- customobtained by the same production process as in Preparation Example 1
- customwas carried out at −20° C.
出典と根拠
- ORDレコード
- ord-c052af79372e407e871aca501ff7e6ec
- 出典データセット
- uspto-grants-2007_01
- 特許番号
- US07169944B2
反応ノート
読み込み中…