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Formic Acid → ethyl (3R)-1-methylpiperidine-3-carboxylate

HRID 454001
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HRID 454001 반응식
[NH:1]1[CH2:11][CH2:10][CH2:9][C@@H:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[CH2:2]1.[CH:12](O)=O.C(=O)([O-])O.[Na+].[OH-].[Na+]>C=O>[CH3:12][N:1]1[CH2:11][CH2:10][CH2:9][C@@H:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[CH2:2]1
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참가 물질

6

반응물 4

HCID 284Formic AcidHCID 14798Sodium HydroxideHCID 185582ethyl (3R)-piperidine-3-carboxylateHCID 516892Sodium Bicarbonate

생성물 1

HCID 736036ethyl (3R)-1-methylpiperidine-3-carboxylate수율 73%

시약·촉매·용매 1

HCID 712Formaldehyde용매

실험 절차

(R)-Ethyl nipecotate (5.7 g 365 mmol), (prepared by resolution of ethyl nipecotate by treatment with L(+)-tartaric acid as described in J. Org. Chem. 1991, (56), 1168), was dissolved in 38.5% aqueous formaldehyde solution (45 ml) and formic acid (90 ml) and the mixture heated at reflux for 18 hours. The mixture was allowed to cool and added dropwise to cooled saturated aqueous sodium hydrogen carbonate solution. The mixture was adjusted to pH12 by addition of sodium hydroxide and the mixture was extracted with methylene chloride. The organic extract was washed with brine, dried (MgSO4) and the solvent removed by evaporation to give (R)-ethyl 1-methylpiperidine-3-carboxylate (4.51 g, 73%) as a colourless oil.

후처리

  1. temperatureat reflux for 18 hours
  2. temperatureto cool
  3. additionadded dropwise
  4. extractionthe mixture was extracted with methylene chloride
  5. extractionThe organic extract
  6. washwas washed with brine
  7. dry with materialdried (MgSO4)
  8. customthe solvent removed by evaporation

출처 및 근거

ORD 기록
ord-9aadfca64f224018952b4241356f9dbd
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08492560B2

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