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Sodium Hydroxide → (R)-2-Methyl-2-(1-methyl-piperidin-3-yl)-propionic acid

HRID 252387
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인쇄 미리보기

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HRID 252387 반응식
C[O:2][C:3](=[O:14])[C:4]([CH3:13])([C@H:6]1[CH2:11][CH2:10][CH2:9][N:8]([CH3:12])[CH2:7]1)[CH3:5].[OH-].[Na+]>CO>[CH3:13][C:4]([C@H:6]1[CH2:11][CH2:10][CH2:9][N:8]([CH3:12])[CH2:7]1)([CH3:5])[C:3]([OH:14])=[O:2]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 66889160(R)-2-methyl-2-(1-methyl-piperidin-3-yl)-propionic acid methyl ester

생성물 1

HCID 66888436(R)-2-Methyl-2-(1-methyl-piperidin-3-yl)-propionic acid

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
60 °C

실험 절차

0.489 g of (R)-2-methyl-2-(1-methyl-piperidin-3-yl)-propionic acid methyl ester are taken up in 4 ml of methanol and the mixture is admixed with 4 ml of 3M NaOH. The mixture is then stirred at 60° C. for 6 hours. The methanol is removed in vacuo and the aqueous residue acidified with 2M HCl to pH 7. The mixture is concentrated under reduced pressure. The residue is taken up in 10 ml of ethanol and the insoluble salts removed by filtration. Concentration of the filtrate under reduced pressure provides the title compound as a colourless solid which can be used without further purification.

후처리

  1. customThe methanol is removed in vacuo
  2. concentrationThe mixture is concentrated under reduced pressure
  3. customthe insoluble salts removed by filtration

출처 및 근거

ORD 기록
ord-d52a6931ade74632b5735472a87539ca
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07868036B2

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