Lithium Hydroxide → 1-[(Tert-butoxy)carbonyl]-4-ethylpiperidine-4-carboxylic acid

HRID 1822601노트

반응식

HRID 1822601 반응식
C([O:3][C:4](=[O:20])[C:5]1([CH2:18][CH3:19])[CH2:10][CH2:9][N:8]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH2:7][CH2:6]1)C.[OH-].[Li+]>C(O)C>[C:14]([O:13][C:11]([N:8]1[CH2:9][CH2:10][C:5]([CH2:18][CH3:19])([C:4]([OH:20])=[O:3])[CH2:6][CH2:7]1)=[O:12])([CH3:17])([CH3:16])[CH3:15]

참가 물질

4

반응물 2

HCID 3939Lithium HydroxideHCID 53393415Ethyl 1-Boc-4-ethyl-4-piperidine carboxylate

생성물 1

HCID 221690971-[(Tert-butoxy)carbonyl]-4-ethylpiperidine-4-carboxylic acid수율 45.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 1-tert-butoxycarbonyl-4-ethylisonipecotic acid ethyl ester (570 mg) in ethanol (10 ml) was added a 1M lithium hydroxide solution (8 ml), and the mixture was refluxed under heating for 20 hours. Then, the reaction mixture was concentrated, and water was added to the residue. The aqueous layer was washed with ether acidified with 1N hydrochloric acid, and extracted with ether. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give the title compound (233 mg, yield 45%).

후처리

  1. temperaturethe mixture was refluxed
  2. temperatureunder heating for 20 hours
  3. concentrationThen, the reaction mixture was concentrated
  4. additionwater was added to the residue
  5. washThe aqueous layer was washed with ether
  6. extractionextracted with ether
  7. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-7ce88c7dda5943938f45e77c9310bb97
출처 데이터셋
uspto-grants-2006_05
특허 번호
USRE039088E1

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