2,3-Dimethylphenol → 4-(2,3-Dimethylphenoxy)butanoic acid

HRID 341349ノート

反応式

HRID 341349 の反応式
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[OH:9].[O-]CC.[Na+].Br[CH2:15][CH2:16][CH2:17][C:18]([O:20]CC)=[O:19].[OH-].[Na+]>C(O)C.O>[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[O:9][CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19]

参加物

7

反応物 4

HCID 106872,3-DimethylphenolHCID 14798Sodium HydroxideHCID 76300Ethyl 4-bromobutyrateHCID 2723922Sodium ethoxide

生成物 1

HCID 16225244-(2,3-Dimethylphenoxy)butanoic acid

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒2 回HCID 962Water溶媒2 回

実験手順

2,3-Dimethylphenol (24.5 g, 0.2 mol) was dissolved in 125 ml of anhydrous ethanol. Seventy five (75) ml of 21 wt % sodium ethoxide solution in ethanol (0.2 mol) was added to the solution. The mixture solution was stirred at room temperature for 10 min. Ethyl 4-bromobutyrate (40 g, 0.205 mol) was then added to the solution. The reaction mixture was refluxed at 80° C. for 24 h. The precipitate was filtered of. The filtrate was then mixed with a solution of sodium hydroxide (10 g, 0.25 mol) in 150 ml of water. The mixture was stirred at 70° C. for about 2 hours, and monitored with HPLC. The mixture was diluted with 150 ml of water and acidified to pH 1. Oily precipitate formed immediately. The precipitate was collected by decanting the supernatant and washed with water twice (100 ml×2). The oily precipitate solidified after being kept in water at room temperature overnight.

後処理

  1. temperatureThe reaction mixture was refluxed at 80° C. for 24 h
  2. filtrationThe precipitate was filtered of
  3. stirringThe mixture was stirred at 70° C. for about 2 hours
  4. customOily precipitate formed immediately
  5. customThe precipitate was collected
  6. customby decanting the supernatant
  7. washwashed with water twice (100 ml×2)
  8. waitafter being kept in water at room temperature overnight

出典と根拠

ORDレコード
ord-02f2799bd0824bccadf0a76a277044e8
出典データセット
uspto-grants-2014_11
特許番号
US08895777B2

反応ノート

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