Water → HCID 86689986, 화합물

HRID 1754053노트

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HRID 1754053 반응식
[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]

참가 물질

7

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-82697acceb8a4b98a1a702ddb8f37f63
출처 데이터셋
uspto-grants-2015_10
특허 번호
US09169203B2

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