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Ethanol → (2-Ethyl-2,3-dihydro-1H-inden-5-yl)acetic acid

HRID 261541
ノート
印刷プレビュー

反応式

HRID 261541 の反応式
[CH2:1]([CH:3]1[CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8](CC#N)[CH:9]=2)[CH2:4]1)[CH3:2].[OH-:15].[K+].[CH2:17]([OH:19])[CH3:18]>O>[CH2:1]([CH:3]1[CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([CH2:18][C:17]([OH:15])=[O:19])[CH:9]=2)[CH2:4]1)[CH3:2]
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 702EthanolHCID 14797Potassium HydroxideHCID 12627904(2-Ethyl-2,3-dihydro-1H-inden-5-yl)acetonitrile

生成物 1

HCID 12627894(2-Ethyl-2,3-dihydro-1H-inden-5-yl)acetic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

12.8 g of 2-ethyl-5-indan-acetonitrile are dissolved in 350 cc of ethanol, a solution of 26.7 g of potassium hydroxide in 45 cc of water is added, and the mixture is boiled at reflux for 20 hours. The solution is concentrated to 50 cc, diluted with water and extracted with ether, and the ether phase is discarded. The aqueous phase is then acidified with 2 N hydrochloric acid and extracted with ether. The crude 2-ethyl-5-indanacetic acid, obtained after concentrating the ether extract, is purified by chromatography on a 50-fold quantity of silica gel using chloroform containing 1.5% of methanol as eluant. After recrystallization from hexane the title compound has a M.P. of 44°-46°.

後処理

  1. temperatureat reflux for 20 hours
  2. concentrationThe solution is concentrated to 50 cc
  3. additiondiluted with water
  4. extractionextracted with ether
  5. extractionextracted with ether

出典と根拠

ORDレコード
ord-3282f30a06dd4dd0b61c7f476d4799ca
出典データセット
uspto-grants-1979_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04166131

反応ノート

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