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Potassium Hydroxide → Acetic acid, 5-methoxy-m-tolyl-

HRID 1760015
ノート
印刷プレビュー

反応式

HRID 1760015 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:10][C:11]#N)[CH:6]=[C:7]([CH3:9])[CH:8]=1.[OH-:13].[K+].[OH2:15].CC(O)C>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:10][C:11]([OH:15])=[O:13])[CH:6]=[C:7]([CH3:9])[CH:8]=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

4

反応物 3

HCID 14797Potassium HydroxideHCID 21889133Propan-2-ol--water (1/1)HCID 22048241(3-Methoxy-5-methylphenyl)acetonitrile

生成物 1

HCID 39879Acetic acid, 5-methoxy-m-tolyl-収率 80%

反応条件

温度
120 °C

実験手順

A solution of 3-methoxy-5-methylphenylacetonitrile (9 g; 0.06 mol; from step (ii) above) and KOH (17 g; 0.3 mol) in 150 mL of water:i-PrOH (2:1) was heated while stirring in an autoclave at 120° C. overnight and then at room temperature for 2 days. The reaction mixture was concentrated and extracted with ether. The aqueous phase was acidified and extracted twice with ether. The combined organic layers were washed with water, dried (Na2SO4), and evaporated to a residue which was dissolved in EtOH, treated with activated carbon, filtered, and evaporated to yield the sub-title compound (8.1 g; 80%) as yellow crystals.

後処理

  1. waitat room temperature for 2 days
  2. concentrationThe reaction mixture was concentrated
  3. extractionextracted with ether
  4. extractionextracted twice with ether
  5. washThe combined organic layers were washed with water
  6. dry with materialdried (Na2SO4)
  7. customevaporated to a residue which
  8. dissolutionwas dissolved in EtOH
  9. additiontreated with activated carbon
  10. filtrationfiltered
  11. customevaporated

出典と根拠

ORDレコード
ord-13218de8eb28454cbb91662d2fd9c665
出典データセット
uspto-grants-2005_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06838478B2

反応ノート

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