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Water → 2-(4-(3-Methyl-2-butenyl)phenyl)propionic acid

HRID 1413833
ノート
印刷プレビュー

反応式

HRID 1413833 の反応式
[CH2:1]([C:6]1[CH:11]=[CH:10][C:9]([CH:12]([CH3:15])[C:13]#N)=[CH:8][CH:7]=1)[CH:2]=[C:3]([CH3:5])[CH3:4].[OH-:16].[Na+].[OH2:18]>CO>[CH2:1]([C:6]1[CH:11]=[CH:10][C:9]([CH:12]([CH3:15])[C:13]([OH:18])=[O:16])=[CH:8][CH:7]=1)[CH:2]=[C:3]([CH3:5])[CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 135850232-(p-Prenylphenyl)propionitrile

生成物 1

HCID 1754602-(4-(3-Methyl-2-butenyl)phenyl)propionic acid

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A mixture of 16.4 g of 2-(p-prenylphenyl)propionitrile, 60 g of sodium hydroxide, 100 ml of water and 120 ml of methanol was stirred at 70°-75° C. for 8 hours. The resulting solution was concentrated and acidified with dilute hydrochloric acid, followed by extraction with ethyl ether and washing with water. The ethereal solution was extracted with 5% aqueous potassium hydroxide solution. The aqueous layer was acidified with dilute hydrochloric acid, and extracted with ether, which was then washed with water, dried over anhydrous magnesium sulfate and decolorized with activated charcoal. The ether was removed to give 15.5 g of 2-(p-prenylphenyl)propionic acid. ##STR1##

後処理

  1. concentrationThe resulting solution was concentrated
  2. extractionfollowed by extraction with ethyl ether
  3. washwashing with water
  4. extractionThe ethereal solution was extracted with 5% aqueous potassium hydroxide solution
  5. extractionextracted with ether, which
  6. washwas then washed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customThe ether was removed

出典と根拠

ORDレコード
ord-6ec6a089c769436f80a00e4fd1cac617
出典データセット
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04251543

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート