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Water → 4-[4-(3-Chloro-propoxy)-phenyl]-4-oxo-2-pyridin-2-yl-butyric acid ethyl ester

HRID 2042637
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HRID 2042637 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9].[H-].[Na+].Br[CH2:16][C:17]([C:19]1[CH:24]=[CH:23][C:22]([O:25][CH2:26][CH2:27][CH2:28][Cl:29])=[CH:21][CH:20]=1)=[O:18].O>CN(C)C=O>[CH2:11]([O:10][C:8](=[O:9])[CH:7]([C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=1)[CH2:16][C:17]([C:19]1[CH:24]=[CH:23][C:22]([O:25][CH2:26][CH2:27][CH2:28][Cl:29])=[CH:21][CH:20]=1)=[O:18])[CH3:12]
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참가 물질

6

반응물 4

HCID 962WaterHCID 24758Sodium hydrideHCID 75960Ethyl 2-pyridylacetateHCID 140970932-Bromo-1-[4-(3-chloro-propoxy)-phenyl]-ethanone

생성물 1

HCID 596520644-[4-(3-Chloro-propoxy)-phenyl]-4-oxo-2-pyridin-2-yl-butyric acid ethyl ester

시약·촉매·용매 1

HCID 6228Dimethylformamide
용매
2회

실험 절차

In a 500 mL round bottom flask ethyl 2-pyridylacetate (2.0 g, 12.1 mmol), and 60% sodium hydride (508 mg, 12.7 mmol) in dimethylformamide (50 mL) was stirred 1 h. 2-Bromo-1-[4-(3-chloro-propoxy)-phenyl]-ethanone (3.53 g, 12.1 mmol) was then added in dimethylformamide (50 mL) via dropping funnel. The reaction was stirred 14 h. Water (300 mL) was added and the organics were extracted three times with ethyl acetate, and then dried over MgSO4. Purification with silica gel chromatography eluting with hexanes/ethyl acetate (3:1) produced 2.8 g (62%). MS m/z 376 (M+H).

후처리

  1. extractionthe organics were extracted three times with ethyl acetate
  2. dry with materialdried over MgSO4
  3. customPurification with silica gel chromatography
  4. washeluting with hexanes/ethyl acetate (3:1)
  5. customproduced 2.8 g (62%)

출처 및 근거

ORD 기록
ord-b046712e335048a29786ae3387708d67
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08586588B2

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