Water → HCID 86689986、化合物
反応式
[OH:1][CH:2]([CH2:6][CH2:7][S:8][CH3:9])[C:3]([OH:5])=[O:4].[CH2:10]([OH:24])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23].C1(C)C=C[C:28]([S:31](O)(=O)=O)=CC=1.[OH2:36].[C:37]1(C)C=C[CH:40]=[CH:39][CH:38]=1>C(OCC)(=O)C>[OH:1][CH:2]([CH2:6][CH2:7][S:8][CH3:9])[C:3]([O:5][CH:38]([CH2:39][CH2:40][S:31][CH3:28])[C:37](=[O:36])[O:24][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[O:4]参加物
実験手順
To 2-hydroxy-4-(methylthio)butanoic acid (Alimet 88%) (10.1 g, 59.2 mmol) was added 1-tetradecanol (7.57 g, 35.3 mmol), p-toluenesulfonic acid (0.55 g, 2.9 mmol) in toluene (50 mL) in a round bottom flask that was fitted with a Dean Stark trap and reflux condenser. The resulting mixture was heated to reflux with removal of water overnight. The reaction was cooled to room temperature and then diluted with ethyl acetate (65 mL) and washed with sat. NaHCO3 (3×30 mL), water (1×30 mL), dried over magnesium sulfate, filtered and evaporated to give a dark oil. The oil was purified by silica gel chromatography with 0-30% ethyl acetate/heptane to give a light yellow oil (3.34 g, 24%). 1H NMR (500 MHz, DMSO-d6) δ ppm 0.85 (t, J=6.83 Hz, 3 H) 1.11-1.38 (m, 22 H) 1.56 (t, J=6.20 Hz, 2 H) 1.76-1.99 (m, 2 H) 1.99-2.10 (m, 8 H) 2.51-2.64 (m, 4 H) 3.99-4.15 (m, 2 H) 4.16-4.32 (m, 1 H) 5.00-5.16 (m, 1 H) 5.51-5.69 (m, 1 H).
後処理
- customwas fitted with a Dean Stark trap
- temperaturereflux condenser
- temperatureThe resulting mixture was heated
- washwashed with sat. NaHCO3 (3×30 mL), water (1×30 mL)
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customevaporated
- customto give a dark oil
- customThe oil was purified by silica gel chromatography with 0-30% ethyl acetate/heptane
出典と根拠
- ORDレコード
- ord-82697acceb8a4b98a1a702ddb8f37f63
- 出典データセット
- uspto-grants-2015_10
- 特許番号
- US09169203B2
反応ノート
読み込み中…