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Sodium Cyanide → 2-(2-(Methylthio)phenyl)acetonitrile

HRID 440542
ノート
印刷プレビュー

反応式

HRID 440542 の反応式
P(Br)(Br)Br.[CH3:5][S:6][C:7]1[CH:14]=[CH:13][CH:12]=[CH:11][C:8]=1[CH2:9]O.[C-:15]#[N:16].[Na+]>C1(C)C=CC=CC=1.O.C(O)C>[CH3:5][S:6][C:7]1[CH:14]=[CH:13][CH:12]=[CH:11][C:8]=1[CH2:9][C:15]#[N:16]
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

7

反応物 3

HCID 8929Sodium CyanideHCID 24614Phosphorus tribromideHCID 3551404(2-Methylsulfanylphenyl)methanol

生成物 1

HCID 130200632-(2-(Methylthio)phenyl)acetonitrile

試薬・触媒・溶媒 3

HCID 702Ethanol溶媒HCID 962Water溶媒2 回
HCID 1140
Toluene
溶媒
2 回

反応条件

温度
40 °C

実験手順

Phosphorus tribromide (75 g) in toluene (50 ml) was added to a stirred mixture of 2-methylthiobenzyl alcohol (42.5 g) in toluene (25 ml) over 10 minutes at 5° C. The mixture was then stirred at 40° C. for 1 hour, water (100 ml) was added and stirring continued at ambient temperature for 1 hour. The organic layer was separated and the aqueous layer extracted with ethyl acetate. The combined organic layers yielded an oil. The oil (58.6 g) was dissolved in a 1:2 mixture of water and ethanol and sodium cyanide (26.5 g) was added over 15 minutes. The mixture was stirred at 50° C. for 1.5 hours then poured onto water (500 ml) and extracted with ethyl acetate. The extract yielded 2-methylthiophenylacetonitrile.

後処理

  1. stirringstirring
  2. waitcontinued at ambient temperature for 1 hour
  3. customThe organic layer was separated
  4. extractionthe aqueous layer extracted with ethyl acetate
  5. customThe combined organic layers yielded an oil
  6. additionwas added over 15 minutes
  7. stirringThe mixture was stirred at 50° C. for 1.5 hours
  8. additionthen poured onto water (500 ml)
  9. extractionextracted with ethyl acetate

出典と根拠

ORDレコード
ord-2bbfef484914458e8f84be195ffb7257
出典データセット
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05519034

反応ノート

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