Phenol → 4-(3-Pyridylmethyl)phenoxyacetic acid ethyl ester

HRID 2058516ノート

反応式

HRID 2058516 の反応式
[C:1]1([OH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[Na+].Br[CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13].[CH3:17][N:18]([CH3:21])C=O>>[CH2:15]([O:14][C:12](=[O:13])[CH2:11][O:7][C:1]1[CH:6]=[CH:5][C:4]([CH2:3][C:2]2[CH:17]=[N:18][CH:21]=[CH:6][CH:1]=2)=[CH:3][CH:2]=1)[CH3:16]

参加物

5

反応物 4

HCID 996PhenolHCID 6228DimethylformamideHCID 7748Ethyl bromoacetateHCID 24758Sodium hydride

生成物 1

HCID 544292054-(3-Pyridylmethyl)phenoxyacetic acid ethyl ester

反応条件

温度
100 °C

実験手順

A mixture of 0.70 g of the phenol compound(prepared as described in Example 9), 0.30 g of sodium hydride (content 63%) and 14 ml of N,N-dimethylformamide was stirred at 100° C. for 20 minutes, and stirred with 0.64 g of ethyl bromoacetate at 70° C. for 2 hours. The reaction mixture was concentrated under reduced pressure, the residue was dissolved in water, and extracted with diethyl ether. The extract was washed with water, and a saturated aqueous solution of sodium chloride, dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a 0.5% V/V solution of ethanol in chloroform as eluent to give 0.166 g of the title compound having the following physical characteristics:

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. dissolutionthe residue was dissolved in water
  3. extractionextracted with diethyl ether
  4. washThe extract was washed with water
  5. dry with materiala saturated aqueous solution of sodium chloride, dried over sodium sulphate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by column chromatography on silica gel using a 0.5% V/V solution of ethanol in chloroform as eluent

出典と根拠

ORDレコード
ord-6c528b7701c44f04aceb9028500f958a
出典データセット
uspto-grants-1982_03
特許番号
US04317828

反応ノート

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