1-Phenylethanol, (R)- → (alphaR)-alpha-Methylcyclohexanemethanol
反応式
[CH3:1][C@@H:2]([OH:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>C(O)(C)C>[CH:3]1([C@H:2]([OH:9])[CH3:1])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1参加物
3
実験手順
An autoclave was charged with (R)-alpha-methylbenzyl alcohol (980 g, synthesized as above) and isopropanol (100 g). Catalyst RuO2.H2O (0.2 g) was then added, and the reaction mixture was hydrogenated at a pressure of 20 bar and a temperature ranging from 70 to 80° C. for 4 hours. The catalyst was filtered. The organic layer was distilled first at 100 mmHg to remove isopropanol, and then at 5-10 mmHg to provide (R)-1-cyclohexylethanol (913 g) (optical rotation: [α]D−4.31°; optical purity: 83.3% ee).
後処理
- filtrationThe catalyst was filtered
- distillationThe organic layer was distilled first at 100 mmHg
- customto remove isopropanol
出典と根拠
- ORDレコード
- ord-22f385a1eea34b8c83fbce884ffe5539
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US07993633B2
反応ノート
読み込み中…