3-(6-Benzyloxynaphthalen-2-yl)pentan-3-ol → 6-(1-Ethyl-1-hydroxypropyl)naphthalen-2-ol
反応式
C([O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[CH:15]=[C:14]([C:19]([OH:24])([CH2:22][CH3:23])[CH2:20][CH3:21])[CH:13]=[CH:12]2)C1C=CC=CC=1.[H][H]>C(O)C>[CH2:20]([C:19]([C:14]1[CH:15]=[C:16]2[C:11](=[CH:12][CH:13]=1)[CH:10]=[C:9]([OH:8])[CH:18]=[CH:17]2)([OH:24])[CH2:22][CH3:23])[CH3:21]参加物
4
実験手順
Treat a mixture of 3-(6-benzyloxynaphthalen-2-yl)pentan-3-ol (1.5 g, 4.68 mmol) and 5% PdlAl2CO3 (0.90 g) in ethanol (750 mL) with hydrogen at 60 psi for 8 h at RT. Filter the catalyst from the reaction mixture and concentrate the filtrate to give the title compound as a yellow solid (0.94 g, 87%). MS (ES) m/e 229 (M−1).
後処理
- additionTreat
- filtrationFilter the catalyst from the reaction mixture
- concentrationconcentrate the filtrate
出典と根拠
- ORDレコード
- ord-1107ca8228d24d54b4d616d75be2ef36
- 出典データセット
- uspto-grants-2011_05
- 特許番号
- US07943795B2
反応ノート
読み込み中…