4-Methoxybenzaldehyde → Cyclohexyl-(4-methoxyphenyl)methanol
反応式
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[CH:5][CH:4]=1.[CH:11]1([Mg]Br)[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1>>[CH:11]1([CH:7]([C:6]2[CH:9]=[CH:10][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)[OH:8])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1参加物
3
実験手順
Referring now to FIG. 2, this alternative synthesis starts from 4-methoxy-benzaldehyde (VI) which is subjected to treatment with cyclohexyl magnesium bromide to yield cyclohexyl-(4-methoxy-phenyl)-methanol (V). This in turn is then oxidised so as to yield cyclohexyl-(4-methoxy-phenyl)-methanone (III).
後処理
- customthis alternative synthesis
出典と根拠
- ORDレコード
- ord-aacd95c11a9f4f8eb70c139deb24342e
- 出典データセット
- uspto-grants-2004_06
- 特許番号
- US06756502B2
反応ノート
読み込み中…