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Gamma-Butyrolactone → 4-((3-Bromophenyl)thio)butanoic acid

HRID 37415
ノート
印刷プレビュー

反応式

HRID 37415 の反応式
[Na].[Br:2][C:3]1[CH:4]=[C:5]([SH:9])[CH:6]=[CH:7][CH:8]=1.[C:10]1(=[O:15])[O:14][CH2:13][CH2:12][CH2:11]1>C(O)C>[Br:2][C:3]1[CH:4]=[C:5]([S:9][CH2:13][CH2:12][CH2:11][C:10]([OH:15])=[O:14])[CH:6]=[CH:7][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

5

反応物 3

HCID 7302Gamma-ButyrolactoneHCID 80597m-BromobenzenethiolHCID 5360545Sodium

生成物 1

HCID 545154194-((3-Bromophenyl)thio)butanoic acid

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
110 °C

実験手順

3.74 g of sodium were dissolved in 77 ml of absolute ethanol under argon. The solution was treated dropwise with 25 g of m-bromothiophenol and heated to reflux. Thereafter, 12.4 ml of γ-butyrolactone were added and the reaction mixture was heated to 110° C. for 5 hours. The separated carboxylic acid sodium salt was removed by filtration, washed with a small amount of ether and dissolved in 300 ml of water. The solution was acidified to pH 2 with 1N HCl while cooling with ice, the free carboxylic acid was extracted with ether, the ethereal solution was dried and evaporated. There were obtained 33.1 g of 4-(m-bromophenylmercapto)butyric acid.

後処理

  1. temperatureheated to reflux
  2. customThe separated carboxylic acid sodium salt was removed by filtration
  3. washwashed with a small amount of ether
  4. dissolutiondissolved in 300 ml of water
  5. temperaturewhile cooling with ice
  6. extractionthe free carboxylic acid was extracted with ether
  7. customthe ethereal solution was dried
  8. customevaporated

出典と根拠

ORDレコード
ord-6cb72450fdfa4b8d8d6fea27607b02ae
出典データセット
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05420273

反応ノート

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