Water → tert-Butyl 3-ethyl-4-oxopiperidine-1-carboxylate

HRID 917112노트

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HRID 917112 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11](=[O:14])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].N1CC[CH2:17][CH2:16]1.O.ICC>C1C=CC=CC=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH2:10][C:11](=[O:14])[CH:12]([CH2:16][CH3:17])[CH2:13]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

참가 물질

7

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온도
100 °C

실험 절차

A solution of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (5 g, 25.1 mmol), pyrollidine (5 mL) and p-toluenesulfonic acid (25 mg) in benzene (100 mL) was heated at reflux for 16 h with azeotropic distillation of water. The resulting enamine solution was cooled to rt and concentrated. The crude enamine was dissolved in acetonitrile (50 mL); iodoethane (4.67 g, 30.1 mmol.) was added and the mixture was heated at 100° C. for 0.5 h, cooled to rt and concentrated. The mixture was dissolved in ethyl acetate (200 mL), washed with 1 N hydrochloric acid, saturated aqueous sodium bicarbonate, and brine. The extract was dried over magnesium sulfate, filtered and concentrated. The crude compound was purified by silica gel chromatography (80% hexanes/20% ethyl acetate) to afford 3-ethyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester (680 mg).

후처리

  1. concentrationconcentrated
  2. dissolutionThe crude enamine was dissolved in acetonitrile (50 mL)
  3. temperaturecooled to rt
  4. concentrationconcentrated
  5. dissolutionThe mixture was dissolved in ethyl acetate (200 mL)
  6. washwashed with 1 N hydrochloric acid, saturated aqueous sodium bicarbonate, and brine
  7. dry with materialThe extract was dried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe crude compound was purified by silica gel chromatography (80% hexanes/20% ethyl acetate)

출처 및 근거

ORD 기록
ord-90daccaef7a440e1b1ac8895cf24635f
출처 데이터셋
uspto-grants-2007_09
특허 번호
US07271176B2

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