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Sodium Cyanide → 4-(Trifluoromethylthio)phenylacetonitrile

HRID 894542
ノート
印刷プレビュー

反応式

HRID 894542 の反応式
[C-:1]#[N:2].[Na+].[F:4][C:5]([S:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13]Cl)=[CH:11][CH:10]=1)([F:7])[F:6]>O.[Cl-].C([N+](CC)(CC)CC)C>[F:4][C:5]([S:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13][C:1]#[N:2])=[CH:11][CH:10]=1)([F:7])[F:6]
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 2

HCID 8929Sodium CyanideHCID 27831641-(Chloromethyl)-4-((trifluoromethyl)sulfanyl)benzene

生成物 1

HCID 27779054-(Trifluoromethylthio)phenylacetonitrile収率 123.3%

試薬・触媒・溶媒 2

HCID 5946Tetraethylammonium Chloride触媒HCID 962Water溶媒2 回

反応条件

温度
110 °C

実験手順

75 g of sodium cyanide were dissolved in 200 ml of water, and 15 g of tetraethylammonium chloride after 450 g of 4-trifluoromethylmercapto-benzyl chloride were added. The reaction mixture was stirred at 110° C. for 1 hour and then cooled. The cold mixture was diluted with 200 ml of water and then extracted twice with methylene chloride. After drying the organic phase, the solvent was distilled off and the crude product was purified by distillation. 410 g of 4-trifluoromethylmercapto-benzyl cyanide were obtained. Boiling point=95°-97° C./1.5 mm Hg; nD20 =1.5025.

後処理

  1. temperaturecooled
  2. extractionextracted twice with methylene chloride
  3. customAfter drying the organic phase
  4. distillationthe solvent was distilled off
  5. distillationthe crude product was purified by distillation

出典と根拠

ORDレコード
ord-2c37f3add20f4cfb88092aad0eccb7a6
出典データセット
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04284643

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート