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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484319Generated: October 25, 2026

Carbon Dioxide → HCID 178448133, compound

https://huagongshe.com/reaction/484319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2,3-DifluorophenolHCID 80879—
Reactant4-Ethoxy-2,3-difluorobenzoic acidHCID 2769400—
Reactant1-Ethoxy-2,3-DifluorobenzeneHCID 2782928—
ReactantDiethyl sulfate potassium carbonateHCID 86747043—
ReactantHCID 178448131HCID 178448131—
ReactantHCID 178483778HCID 178483778—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178448133HCID 178448133—

Reaction Steps

0.1 mol of 2,3-difluoro-4-ethoxybenzoic acid (preparable from 2,3-difluorophenol by alkylation using diethyl sulfate/potassium carbonate in dimethylformamide, metallation of the 2,3-difluorophenetole in the 4-position using butyllithium/tetramethylethylenediamine in tetrahydrofuran (THF) at -70° to -80° and reaction with solid carbon dioxide), 0.01 mol of 4-dimethylaminopyridine and 0.1 mol of trans-4-propylcyclohexanol are initially introduced in 150 ml of dichloromethane, a solution of 0.1 mol of dicyclohexylcarbodiimide in 30 ml of dichloromethane is added dropwise at 10° with stirring, and the mixture is subsequently stirred at room temperature for 15 hours. The mixture is filtered through silica gel with suction, the solvent is evaporated, and trans-4-propylcyclohexyl 2,3-difluoro-4-ethoxybenzoate is obtained as a residue and is purified by crystallization. Mp. 93°, cp. (48°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05230827
Source datasetuspto-grants-1993_07
ORD IDord-c0a7ba1d70d94fcfa35835ddd9b19302
Source noteuspto-grants-1993_07