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Trifluoroacetic acid → 2,2-Dimethyl-3-(piperidine-4-yl)-propionic acid methyl ester

HRID 1641777
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반응식

HRID 1641777 반응식
[CH3:1][O:2][C:3](=[O:21])[C:4]([CH3:20])([CH3:19])[CH2:5][CH:6]1[CH2:11][CH2:10][N:9](C(OC(C)(C)C)=O)[CH2:8][CH2:7]1.FC(F)(F)C(O)=O>C(Cl)Cl>[CH3:1][O:2][C:3](=[O:21])[C:4]([CH3:19])([CH3:20])[CH2:5][CH:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 592610682,2-dimethyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester

생성물 1

HCID 592610232,2-Dimethyl-3-(piperidine-4-yl)-propionic acid methyl ester수율 93%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

2,2-dimethyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester (598 mg) from above was dissolved in methylene chloride (2 mL) and trifluoroacetic acid (1 mL) was added. The mixture was stirred at room temperature for 1 hr and the solvents were evaporated. The mixture was partitioned between ether and sodium hydroxide solution (1N). The organic layer was washed with brine and dried. Evaporation of solvents gave 2,2-dimethyl-3-(piperidine-4-yl)-propionic acid methyl ester (370 mg) as an oil.

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후처리

  1. customthe solvents were evaporated
  2. customThe mixture was partitioned between ether and sodium hydroxide solution (1N)
  3. washThe organic layer was washed with brine
  4. customdried
  5. customEvaporation of solvents

출처 및 근거

ORD 기록
ord-5d8aa55a5ef34c2f82b6f7296850b9e5
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08115011B2

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