Acetic Acid → 2,2-Dimethyl-4-oxocyclopentane-1-carboxylic acid

HRID 1854332노트

반응식

HRID 1854332 반응식
[CH3:1][C:2]1([CH3:8])[CH2:6][C:5](=[O:7])[CH:4]=[CH:3]1.[C-]#N.[K+].C[C:13]([OH:15])=[O:14]>CCO.O>[CH3:1][C:2]1([CH3:8])[CH2:6][C:5](=[O:7])[CH2:4][CH:3]1[C:13]([OH:15])=[O:14]

참가 물질

6

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온도
40 °C

실험 절차

To a solution of 4,4-dimethylcyclopent-2-enone (2.0 g, 18 mmol) in EtOH (50 mL), water (7.5 mL) and AcOH (1.5 mL) was added potassium cyanide (2.36 g, 36.3 mmol). The reaction mixture was heated to about 40° C. and after about 15 h the reaction mixture was concentrated under reduced pressure. The residue was diluted with EtOAc (50 mL) and washed with brine. The organic layer was separated, dried over anhydrous Na2SO4, filtered, and concentrated. The residue was dissolved in aqueous HCl (6N, 50 mL) and heated to reflux. After about 3 days the reaction mixture was cooled to room temperature and concentrated under reduced pressure to provide 2,2-dimethyl-4-oxocyclopentanecarboxylic acid (3.7 g, 90%, ˜70% purity by 1H NMR) that was carried on without additional purification: LC/MS (Table 2, Method a) Rt=1.30 min; MS m/z: 155 (M−H)−.

후처리

  1. concentrationwas concentrated under reduced pressure
  2. additionThe residue was diluted with EtOAc (50 mL)
  3. washwashed with brine
  4. customThe organic layer was separated
  5. dry with materialdried over anhydrous Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. dissolutionThe residue was dissolved in aqueous HCl (6N, 50 mL)
  9. temperatureheated to reflux
  10. temperatureAfter about 3 days the reaction mixture was cooled to room temperature
  11. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e122ff7ed0ec4f6a95744a1a8b88209b
출처 데이터셋
uspto-grants-2015_02
특허 번호
US08962629B2

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