Water → 4-aminocarbonyl-N-(4-propoxyphenylmethyl)piperidine

HRID 866053노트

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HRID 866053 반응식
[NH2:1][C:2]([CH:4]1[CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1)=[O:3].[CH2:10]([O:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20]Cl)=[CH:16][CH:15]=1)[CH2:11][CH3:12].C(=O)(O)[O-].[K+].O>C1(C)C=CC=CC=1>[NH2:1][C:2]([CH:4]1[CH2:9][CH2:8][N:7]([CH2:20][C:17]2[CH:18]=[CH:19][C:14]([O:13][CH2:10][CH2:11][CH3:12])=[CH:15][CH:16]=2)[CH2:6][CH2:5]1)=[O:3]

참가 물질

6

실험 절차

The method taught by R. A. Farr et al, J. Org. Chem. 1981, 46, 1212-1215, was used in the following two-step preparation. A vigorously stirred solution of 16.5 grams (0.129 mole) of 4-aminocarbonylpiperidine, 25.0 grams (0.135 mole) of 4-propoxyphenylmethyl chloride, and 19.4 grams (0.193 mole) of potassium bicarbonate in 200 mL of toluene was heated at reflux for 6.5 hours. The reaction mixture was then cooled, water was added, and the mixture was extracted with ethyl acetate. The extract was washed with two portions of an aqueous solution saturated with sodium chloride. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to a solid residue, which was slurried in pentane and collected by filtration, yielding 28.2 grams of 4-aminocarbonyl-N-(4-propoxyphenylmethyl)piperidine, mp 142°-146° C. The NMR spectrum was consistent with the proposed structure.

후처리

  1. custom1981, 46, 1212-1215, was used in the following two-step preparation
  2. temperatureat reflux for 6.5 hours
  3. temperatureThe reaction mixture was then cooled
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe extract was washed with two portions of an aqueous solution saturated with sodium chloride
  6. dry with materialThe organic layer was dried with sodium sulfate
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated under reduced pressure to a solid residue, which
  9. filtrationcollected by filtration

출처 및 근거

ORD 기록
ord-0bdf3c4da8a24475917f7120ee4b3488
출처 데이터셋
uspto-grants-1996_10
특허 번호
US05569664

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