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4-Bromo-2-hydroxypyridine → 4-Bromo-2-(3-methoxypropoxy)pyridine

HRID 252355
ノート
印刷プレビュー

反応式

HRID 252355 の反応式
I[CH2:2][CH2:3][CH2:4][O:5][CH3:6].[Br:7][C:8]1[CH:13]=[CH:12][NH:11][C:10](=[O:14])[CH:9]=1>C1C=CC=CC=1.C(=O)([O-])[O-].[Ag+2]>[Br:7][C:8]1[CH:13]=[CH:12][N:11]=[C:10]([O:14][CH2:2][CH2:3][CH2:4][O:5][CH3:6])[CH:9]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 8171154-Bromo-2-hydroxypyridineHCID 135229891-Iodo-3-methoxypropane

生成物 1

HCID 231494694-Bromo-2-(3-methoxypropoxy)pyridine

試薬・触媒・溶媒 2

HCID 178418647HCID 178418647、化合物触媒HCID 241Benzene溶媒

反応条件

温度
45 °C

実験手順

11 mmol of silver carbonate and 20 mmol of 1-iodo-3-methoxypropane [61542-10-7] are added under an argon atmosphere to a solution of 21 mmol of 4-bromo-1H-pyridin-2-one [36953-37-4] in 30 ml of benzene. The reaction mixture is heated to 45° C. with exclusion of light for 2 days. The mixture is cooled to room temperature and filtered through Hyflo. The filtercake is washed with benzene and with saturated aqueous sodium hydrogencarbonate solution. The phases of the filtrate are separated and the aqueous phase is extracted with dichloromethane (3×). The combined organic phases are dried over sodium sulphate and concentrated by evaporation. The title compound is identified on the basis of the Rf value by means of flash chromatography (SiO2 60F).

後処理

  1. temperatureThe mixture is cooled to room temperature
  2. filtrationfiltered through Hyflo
  3. washThe filtercake is washed with benzene and with saturated aqueous sodium hydrogencarbonate solution
  4. customThe phases of the filtrate are separated
  5. extractionthe aqueous phase is extracted with dichloromethane (3×)
  6. dry with materialThe combined organic phases are dried over sodium sulphate
  7. concentrationconcentrated by evaporation

出典と根拠

ORDレコード
ord-5d5145d6c9154d2faefc3380389083d5
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07868036B2

反応ノート

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