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Acetic Acid → 2-(2-Hydroxyphenyl)acetonitrile

HRID 1576896
ノート
印刷プレビュー

反応式

HRID 1576896 の反応式
[OH:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4]O.C(O)(=O)C.[C-:14]#[N:15].[K+]>CS(C)=O>[OH:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4][C:14]#[N:15]
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 176Acetic AcidHCID 5146Salicyl AlcoholHCID 9032Potassium Cyanide

生成物 1

HCID 105828242-(2-Hydroxyphenyl)acetonitrile

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

反応条件

温度
125 °C

実験手順

29.8g of 2-hydroxybenzyl alcohol are dissolved in 250 ml of dimethylsulfoxide, together with 18g of potassium cyanide, and the mixture is heated to 125°C. 16g of glacial acetic acid are then added dropwise over the course of 1 hour and the mixture is stirred for a further 2 hours at 125°C. The dimethylsulfoxide is removed in vacuo and the residue is stirred with 200 ml of water and 150 ml of chloroform. The chloroform phase is separated off and the aqueous phase is re-extracted with 150 ml of chloroform. The combined chloroform phases are extracted by shaking with water and dried with sodium sulfate. After distilling off the chloroform, an oil remains, which solidifies on cooling. Yield: 19.8g = 60.5% of theory. Recrystallization from benzene/ligroin: melting point 118°C.

後処理

  1. customThe dimethylsulfoxide is removed in vacuo
  2. stirringthe residue is stirred with 200 ml of water and 150 ml of chloroform
  3. customThe chloroform phase is separated off
  4. extractionthe aqueous phase is re-extracted with 150 ml of chloroform
  5. extractionThe combined chloroform phases are extracted
  6. stirringby shaking with water
  7. dry with materialdried with sodium sulfate
  8. distillationAfter distilling off the chloroform
  9. temperatureon cooling
  10. customRecrystallization from benzene/ligroin

出典と根拠

ORDレコード
ord-b2acf263902d4f469be9ff6a0ebd0879
出典データセット
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03983160

反応ノート

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