反応 #6427

ord-82e83c02b9134508a72b2b79ba90c519

反応方程式

CC(C)(C)OO
t-butyl hydroperoxide
[Li][CH2]CCC
butyllithium
C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
CCCCCCOc1ccc(C(=O)O)cc1
4-hexyloxybenzoic acid
CN(C)c1ccccn1
dimethylaminopyridine
CCCCCCCCOc1ccc(O)c(F)c1F
2,3-difluoro-4octyloxyphenol
CCCCCC(F)C(F)COc1ccccc1
2,3-difluorooctyloxybenzene
CC(C)(C)OOC(C)(C)C.[Li]
lithium t-butylperoxide
CCCCCCCCOc1ccc(OC(=O)c2ccc(OCCCCCC)cc2)c(F)c1F
2,3-difluoro-4-octyloxyphenyl 4-hexyloxybenzoate

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The mixture is filtered through silica gel
  2. 2
    その他the solvent is evaporated

実験手順

0.1 mol of 4-hexyloxybenzoic acid, 0.01 mol of dimethylaminopyridine and 0.1 mol of 2,3-difluoro-4octyloxyphenol (preparable from 2,3-difluorooctyloxybenzene by lithiation at -70° to -80° and dropwise addition of a solution of lithium t-butylperoxide in ether prepared from 0.12 mol of t-butyl hydroperoxide and 0.12 mol of butyllithium) are introduced into 150 ml of dichloromethane, a solution of 0.1 mol of dicyclohexylcarbodiimide in 30 ml of dichloromethane is added dropwise with stirring at 10o, and the mixture is subsequently stirred at room temperature for 15 hours. The mixture is filtered through silica gel, the solvent is evaporated, and 2,3-difluoro-4-octyloxyphenyl 4-hexyloxybenzoate is obtained as the residue.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05248447uspto-grants-1993_09