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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256912Generated: November 2, 2026

Ethyl chloroformate → Ethyl 2,6-dichloro-4-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/2256912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-3,5-dichlorobenzotrifluorideHCID 1268256—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductEthyl 2,6-dichloro-4-(trifluoromethyl)benzoateHCID 5431530677.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium (1.6M in hexane, 330 ml) was added dropwise with stirring to a solution of 2,6-dichloro-4-trifluoromethylbromobenzene (163.3 g) in ether while maintaining the temperature below -70° C. The mixture was stirred for 1 hour at -78° C. then ethyl chloroformate (61.7 g) was added while maintaining the temperature below -70° C. The mixture was stirred at room temperature overnight. It was cooled to 0° C. and a saturated aqueous solution of ammonium chloride was added. The layers were separated and the organic layer was washed with water, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness and the residue was distilled to give ethyl 2,6-dichloro4-trifluoromethylbenzoate (123.9 g) as a colourless liquid bp 90°-96° C. at 5 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656573
Source datasetuspto-grants-1997_08
ORD IDord-c0b6de3b67f84c83919b719ac23c1a22
Source noteuspto-grants-1997_08