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Sodium Hydroxide → (2RS,5RS)-1-methanesulfonyl-piperidine-2,5-dicarboxylic acid 2-methyl ester

HRID 458377
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반응식

HRID 458377 반응식
[CH3:1][O:2][C:3]([CH:5]1[CH2:10][CH2:9][CH:8]([C:11]([O:13]C)=[O:12])[CH2:7][N:6]1[S:15]([CH3:18])(=[O:17])=[O:16])=[O:4].[OH-].[Na+]>CO.O>[CH3:1][O:2][C:3]([CH:5]1[CH2:10][CH2:9][CH:8]([C:11]([OH:13])=[O:12])[CH2:7][N:6]1[S:15]([CH3:18])(=[O:17])=[O:16])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 69427827HCID 69427827, 화합물

생성물 1

HCID 69433575(2RS,5RS)-1-methanesulfonyl-piperidine-2,5-dicarboxylic acid 2-methyl ester수율 38%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

To a solution of (2RS,5RS)-1-methanesulfonyl-piperidine-2,5-dicarboxylic acid dimethyl ester (46.5 g) in methanol (850 ml) and water (85 ml) was added 1 molar sodium hydroxide (166 ml) within 20 minutes at reflux temperature. The reaction mixture was stirred for 45 minutes at reflux, cooled and concentrated. The residue was taken up in water (300 ml) and washed with Et2O. The aqueous phase was acidified with 1 molar HCl (166 ml) and extracted with EtOAc. The organic phase was washed with brine, dried over magnesium sulphate and concentrated. The residue was crystallized from acetone/Et2O to obtain (2RS,5RS)-1-methanesulfonyl-piperidine-2,5-dicarboxylic acid 2-methyl ester (16.8 g) as a colourless solid, mp 130–133° C., MS: 206 (M+-59).

후처리

  1. temperatureat reflux temperature
  2. temperatureat reflux
  3. temperaturecooled
  4. concentrationconcentrated
  5. washwashed with Et2O
  6. extractionextracted with EtOAc
  7. washThe organic phase was washed with brine
  8. dry with materialdried over magnesium sulphate
  9. concentrationconcentrated
  10. customThe residue was crystallized from acetone/Et2O

출처 및 근거

ORD 기록
ord-4f6e26dad25b46f0b527c78da26b4aa7
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07189756B2

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