Water → HCID 86689986、化合物

HRID 1754053ノート

反応式

HRID 1754053 の反応式
[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

7

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

  1. customwas fitted with a Dean Stark trap
  2. temperaturereflux condenser
  3. temperatureThe resulting mixture was heated
  4. washwashed with sat. NaHCO3 (3×30 mL), water (1×30 mL)
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. customevaporated
  8. customto give a dark oil
  9. 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

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