Methyl 6-benzofurancarboxylate → Methyl 2,3-dihydro-1-benzofuran-6-carboxylate
反応式
[O:1]1[C:5]2[CH:6]=[C:7]([C:10]([O:12][CH3:13])=[O:11])[CH:8]=[CH:9][C:4]=2[CH:3]=[CH:2]1>CO.[Pd]>[O:1]1[C:5]2[CH:6]=[C:7]([C:10]([O:12][CH3:13])=[O:11])[CH:8]=[CH:9][C:4]=2[CH2:3][CH2:2]1参加物
4
実験手順
A mixture of methyl benzofuran-6-carboxylate (17.8 g, 100 mmol) and 10% Pd/C (10.5 g) in MeOH was stirred under hydrogen atmosphere at 50 psi for 2 h. The catalyst was removed by filtration. The solvent was removed under reduced pressure to afford the desired methyl 2,3-dihydrobenzofuran-6-carboxylate (17.8 g, 98.5% yield). 1H NMR (400 MHz, CDCl3) δ: 7.57 (d, J=7.6, 1H), 7.40 (s, 1H), 7.23 (d, J=7.6, 1H), 4.61 (t, J=8.8, 2H), 3.89 (s, 3H), 3.25 (t, J=8.8, 2H).
後処理
- customThe catalyst was removed by filtration
- customThe solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-c399ff16d6024c4282a6d42966a22ac5
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08969386B2
反応ノート
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