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

HRID 1838546

反応式

HRID 1838546 の反応式
[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

参加物

6

実験手順

(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 colorless oil. MS-ESI: 172 [MH]30

後処理

  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

出典と根拠

ORDレコード
ord-789c9772a53844409028821bd48c8632
出典データセット
uspto-grants-2004_01
特許番号
US06673803B2

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