Iodoethane → 1-Ethylpiperidine-4-carboxylic acid

HRID 30782

반응식

HRID 30782 반응식
C([O:3][C:4]([CH:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:5])C.I[CH2:13][CH3:14].C(=O)([O-])[O-].[K+].[K+]>C(O)C>[CH2:13]([N:9]1[CH2:8][CH2:7][CH:6]([C:4]([OH:3])=[O:5])[CH2:11][CH2:10]1)[CH3:14]

참가 물질

5

반응물 3

HCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 70770Ethyl 4-piperidinecarboxylate

생성물 1

HCID 187837731-Ethylpiperidine-4-carboxylic acid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To ethylpiperidine-4-carboxylate (1 eq) in ethanol was added iodoethane (1.1 eq) and potassium carbonate (2 eq) and the resulting mixture was refluxed for 16 h. The mixture was then cooled to room temperature and filtered. Ethanol was concentrated and partitioned between methylene chloride and water. The organic layer was then washed with saturated sodium chloride solution, dried with sodium sulfate and concentrated. To it was then added concentrated hydrochloric acid and water (2:1) and the mixture was refluxed for 5 h. The resulting 1-(ethyl)piperidine-4-carboxylic acid was then azeotroped with toluene. MS: MH+=158.

후처리

  1. temperaturethe resulting mixture was refluxed for 16 h
  2. filtrationfiltered
  3. concentrationEthanol was concentrated
  4. custompartitioned between methylene chloride and water
  5. washThe organic layer was then washed with saturated sodium chloride solution
  6. dry with materialdried with sodium sulfate
  7. concentrationconcentrated
  8. additionTo it was then added concentrated hydrochloric acid and water (2:1)
  9. temperaturethe mixture was refluxed for 5 h
  10. customThe resulting 1-(ethyl)piperidine-4-carboxylic acid was then azeotroped with toluene

출처 및 근거

ORD 기록
ord-0428326bde3a4b91ab8e89202e74669f
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07423150B2

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