4-Hydroxycyclohexanecarboxylic acid → 1-(4-Hydroxycyclohexyl)ethanone

HRID 2361886노트

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HRID 2361886 반응식
[CH3:1][Li].[OH:3][CH:4]1[CH2:9][CH2:8][CH:7]([C:10]([OH:12])=O)[CH2:6][CH2:5]1>C1COCC1>[OH:3][CH:4]1[CH2:5][CH2:6][CH:7]([C:10](=[O:12])[CH3:1])[CH2:8][CH2:9]1

참가 물질

4

반응 조건

온도
-78 °C

실험 절차

Methyllithium (1M in THF) (120 mL, 3.5 eq.) was added to a solution of 4-hydroxy-cyclohexanecarboxylic acid (cis/trans mixture) (5.00 g, 1 eq.) in THF (350 mL) at −78° C. After stirring at −78° C. for 45 min, the cooling bath was removed and the resulting mixture was warmed to room temperature and stirred overnight. After total 24 h, the resulting reaction mixture was poured into ice/water (800 mL). This mixture was vigorously stirred. The separated aqueous phase was extracted with MeOH/EtOAc (˜1/20). The combined organic layer was dried over Na2SO4, filtered and concentrated. The crude product was purified by chromatography (50% to 100% EtOAc/hexanes) to give 1-(4-hydroxy-cyclohexyl)-ethanone (2.08 g, 42%).

후처리

  1. customthe cooling bath was removed
  2. temperaturethe resulting mixture was warmed to room temperature
  3. stirringstirred overnight
  4. waitAfter total 24 h
  5. customthe resulting reaction mixture
  6. stirringThis mixture was vigorously stirred
  7. extractionThe separated aqueous phase was extracted with MeOH/EtOAc (˜1/20)
  8. dry with materialThe combined organic layer was dried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe crude product was purified by chromatography (50% to 100% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-ae87b9126d7c40779080b9b916682edf
출처 데이터셋
uspto-grants-2014_04
특허 번호
US08691814B2

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