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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6331Generated: October 23, 2026

tert-Butyl hydroperoxide → 2,3-Difluoro-4-octyloxyphenyl 4-hexyloxybenzoate

https://huagongshe.com/en/reaction/6331

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant4-(Hexyloxy)benzoic acidHCID 70834—
Reactant2,3-Difluoro-4octyloxyphenolHCID 14766703—
Reactant2,3-DifluorooctyloxybenzeneHCID 19103632—
ReactantCID 86747250HCID 86747250—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product2,3-Difluoro-4-octyloxyphenyl 4-hexyloxybenzoateHCID 19103718—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248447
Source datasetuspto-grants-1993_09
ORD IDord-82e83c02b9134508a72b2b79ba90c519
Source noteuspto-grants-1993_09