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Ethyl bromoacetate → Ethyl N-((pyridin-2-yl)methyl)glycinate

HRID 1974921
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HRID 1974921 반응식
C(=O)([O-])[O-].[K+].[K+].[NH2:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1.Br[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18]>CN(C)C=O>[CH2:20]([O:19][C:17]([CH2:16][NH:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)=[O:18])[CH3:21]
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참가 물질

5

반응물 3

HCID 7748Ethyl bromoacetateHCID 11430Potassium CarbonateHCID 195092-Pyridinemethanamine

생성물 1

HCID 13236080Ethyl N-((pyridin-2-yl)methyl)glycinate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Finely powdered potassium carbonate (5.8 g) was suspended in a solution of 2-(aminomethyl)pyridine (3.0 g) and ethyl bromoacetate (3.1 ml) in dimethylformamide (30 ml). The mixture was stirred at room temperature overnight, then poured into ice water. The mixture was extracted with ethyl acetate (50 ml×2) and the organic layer was washed with saturated sodium chloride solution (2 times), dried over magnesium sulfate, and evaporated in vacuo. The residue was purified with a silica gel column chromatography (MeOH:CHCl3 =1:99 as an eluent) to give N-(ethoxycarbonylmethyl)-N-(pyridin-2-ylmethyl)amine (2.30 g).

후처리

  1. extractionThe mixture was extracted with ethyl acetate (50 ml×2)
  2. washthe organic layer was washed with saturated sodium chloride solution (2 times)
  3. dry with materialdried over magnesium sulfate
  4. customevaporated in vacuo
  5. customThe residue was purified with a silica gel column chromatography (MeOH

출처 및 근거

ORD 기록
ord-e0075a6ff27447b6b58ab99230b7b231
출처 데이터셋
uspto-grants-1994_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05284828

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