反応 #2329011

ord-972f32d772e04892a3b0f04e40a8b053

反応方程式

OC1CCCC(O)C1
1,3-Cyclohexanediol
CC#N
acetonitrile
[F-].[K+]
potassium fluoride on alumina
N#Cc1ccc(F)cc1Cl
4-fluoro-2-chloro-benzonitrile
N#Cc1ccc(OC2CCCC(O)C2)cc1Cl
title compound
収率 8.7%
N#Cc1ccc(OC2CCCC(O)C2)cc1Cl
2-Chloro-4-(3-hydroxy-cyclohexyloxy)-benzonitrile
収率 8.7%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他dried round bottom flask under nitrogen
  2. 2
    温度heated
  3. 3
    温度at reflux for 16 h
  4. 4
    抽出was then extracted with water (2×)
  5. 5
    乾燥dried (MgSO4)
  6. 6
    濃縮concentrated
  7. 7
    その他Purification
  8. 8
    洗浄eluting with 10% EtOAc/hex (ethylacetate and hexane)

実験手順

1,3-Cyclohexanediol (116 mg, 1.0 mmole) was added to a flame dried round bottom flask under nitrogen. The flask was then charged with 5 mL of dry acetonitrile, 26 mg of potassium fluoride on alumina (0.1 mmol), and 4-fluoro-2-chloro-benzonitrile (155 mg, 1.0 mmole) and heated at reflux for 16 h. Diethyl ether (15 ml) was added to the reaction mixture, which was then extracted with water (2×), dried (MgSO4) and concentrated. Purification using a chromatotron, eluting with 10% EtOAc/hex (ethylacetate and hexane) provided 22 mg of the title compound. GC/MS: 251 (M/Z for C13H14ClNO2).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07670613B2uspto-grants-2010_03