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Methyl iodide → 5-Bromo-2-methoxy-3-(3-methoxypropoxy)-pyridine

HRID 252362
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인쇄 미리보기

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HRID 252362 반응식
[Br:1][C:2]1[CH:3]=[C:4]([O:9][CH2:10][CH2:11][CH2:12][O:13][CH3:14])[C:5](=[O:8])[NH:6][CH:7]=1.I[CH3:16]>C1C=CC=CC=1.C(=O)([O-])[O-].[Ag+2]>[Br:1][C:2]1[CH:3]=[C:4]([O:9][CH2:10][CH2:11][CH2:12][O:13][CH3:14])[C:5]([O:8][CH3:16])=[N:6][CH:7]=1
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참가 물질

5

반응물 2

HCID 6328Methyl iodideHCID 231494755-bromo-3-(3-methoxypropoxy)-1H-pyridin-2-one

생성물 1

HCID 231494925-Bromo-2-methoxy-3-(3-methoxypropoxy)-pyridine

시약·촉매·용매 2

HCID 178418647HCID 178418647, 화합물촉매HCID 241Benzene용매

반응 조건

온도
45 °C

실험 절차

A mixture of 21 mmol 5-bromo-3-(3-methoxy-propoxy)-1H-pyridin-2-one, 14 mmol silver carbonate and 25 mmol iodomethane in 35 ml of benzene are stirred at 40-50° C. for 24 hours with exclusion of light. The mixture is cooled in an ice bath and the silver salts are removed by filtration. The filtrate is washed with 2% aqueous sodium hydrogencarbonate solution and with water (2×). The organic layer is dried over sodium sulphate, filtered and concentrated. The title compound is obtained from the residue by means of flash chromatography (SiO2 60F) and identified based on its Rf value.

후처리

  1. temperatureThe mixture is cooled in an ice bath
  2. customthe silver salts are removed by filtration
  3. washThe filtrate is washed with 2% aqueous sodium hydrogencarbonate solution and with water (2×)
  4. dry with materialThe organic layer is dried over sodium sulphate
  5. filtrationfiltered
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-859fe21e75bd43249bd83b7a57b50340
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07868036B2

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