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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600850Generated: October 26, 2026

Ethanol → Benzoic acid, 2,6-difluoro-, ethyl ester

https://huagongshe.com/reaction/1600850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPyridineHCID 1049—
Reactant2,6-Difluorobenzoyl chlorideHCID 87438—
SolventDichloromethaneHCID 6344—
ProductBenzoic acid, 2,6-difluoro-, ethyl esterHCID 51963184%

Reaction Conditions

Temperature0 °C

Reaction Steps

2,6-Difluorobenzoyl chloride was diluted with CH2Cl2 (5 ml) and cooled to 0° C. A mixture of EtOH (1.2 ml, 20 mmol) and pyridine (1.6 ml, 20 mmol) was added, dropwise, over 5 minutes to the reaction mixture. The ice bath was removed after 5 minutes and the reaction mixture strirred at 25° C. for 45 min. The solvent and volatiles were evaporated under reduced pressure and the residue was partitioned between 1N HCl and EtOAc (10 ml each). The aqueous phase was separated and extracted with 2×7 ml EtOAc. The combined organic extracts was washed with NaHCO3 (10 ml), brine (7 ml), dried over MgSO4 and concentrated to give 1.562 g ethyl 2,6-difluorobenzoate as an almost colorless oil. (84% yield from steps B and C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977117
Source datasetuspto-grants-1999_11
ORD IDord-1dc86290ed404c099e979d15573fa68d
Source noteuspto-grants-1999_11