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Butyl bromide → 4-Benzyloxy-1-butyl-1H-pyridin-2-one

HRID 2362803
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HRID 2362803 반응식
Br[CH2:2][CH2:3][CH2:4][CH3:5].C(=O)([O-])[O-].[K+].[K+].[CH2:12]([O:19][C:20]1[CH:25]=[CH:24][NH:23][C:22](=[O:26])[CH:21]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(#N)C>[CH2:12]([O:19][C:20]1[CH:25]=[CH:24][N:23]([CH2:2][CH2:3][CH2:4][CH3:5])[C:22](=[O:26])[CH:21]=1)[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8002Butyl bromideHCID 11430Potassium CarbonateHCID 36077244-Benzyloxy-2(1H)-pyridone

생성물 1

HCID 594970724-Benzyloxy-1-butyl-1H-pyridin-2-one수율 98%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

1-Bromobutane (3.75 g, 27.33 mmol) and potassium carbonate (10.3 g, 74.52 mmol) were added to a solution of 4-benzyloxy-1H-pyridin-2-one (5.0 g, 24.84 mmol) in acetonitrile (200 ml) and the mixture was heated at reflux temperature for 16 hours. Subsequently, the reaction mixture was filtered through diatomaceous earth and concentrated in vacuo. The crude residue was then triturated with diethyl ether to yield pure D4 (6.26 g, 98%) as a white solid.

후처리

  1. temperaturethe mixture was heated
  2. temperatureat reflux temperature for 16 hours
  3. filtrationSubsequently, the reaction mixture was filtered through diatomaceous earth
  4. concentrationconcentrated in vacuo
  5. customThe crude residue was then triturated with diethyl ether

출처 및 근거

ORD 기록
ord-919dd74c6f1d41179515fc3840aea1c0
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08691849B2

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