1-Benzyl-4-hydroxy-3-isopropylpiperidine → 4-Hydroxy-3-isopropylpiperidine
反応式
C([N:8]1[CH2:13][CH2:12][CH:11]([OH:14])[CH:10]([CH:15]([CH3:17])[CH3:16])[CH2:9]1)C1C=CC=CC=1>CO.[H][H].[OH-].[Pd+2].[OH-]>[OH:14][CH:11]1[CH2:12][CH2:13][NH:8][CH2:9][CH:10]1[CH:15]([CH3:17])[CH3:16]参加物
5
実験手順
A mixture of 1-benzyl-4-hydroxy-3-isopropylpiperidine (2.9 g, 12.44 mmole) and 20% palladium hydroxide (0.25 g) in methanol (25 ml) was stirred in hydrogen atmosphere (1 atm.) for 24 hr at 30° C. Catalyst was filtered off, washed with methanol, filtrate was concentrated to dryness to give 4-hydroxy-3-isopropylpiperidine as oil. Yield 1.6 g (80%), C8H17NO, m/z 144 (M+1) PMR (CDCl3): 0.9 (6H, m, 2×CH3), 1.1-1.64 (2H, m, CH & H3), 1.66-2.42 (3H, m, H5, & OH, D2O exchangeable), 2.62 (1H, m, H2), 3.02 (2H, m, H6), 3.45 (1H, bs, NH, D2O exchangeable), 3.54 (1H, m, H6), 4.18 (1H, m, H4).
後処理
- filtrationCatalyst was filtered off
- washwashed with methanol, filtrate
- concentrationwas concentrated to dryness
出典と根拠
- ORDレコード
- ord-d71304b05bb34ec88cf5bcdf5425136a
- 出典データセット
- uspto-grants-2003_08
- 特許番号
- US06608078B2
反応ノート
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