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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8111Generated: October 26, 2026

Ethyl chloroformate → 2-bromo-4,6-difluoro-N-carbethoxy aniline

https://huagongshe.com/reaction/8111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant2-Bromo-4,6-DifluoroanilineHCID 136285—
ReactantEthyl acetate hexaneHCID 21226206—
SolventPyridineHCID 1049—
Product2-bromo-4,6-difluoro-N-carbethoxy anilineHCID 1706857594%

Reaction Steps

To a vigorously stirred solution of 2-bromo-4,6-difluoro aniline (100 g, 0.48 mol) in pyridine (400 mL), at 0° C., is added ethyl chloroformate (70 ml, 0.73 mol) at a rate to keep the temperature below 5° C. When addition is complete, the mixture is stirred at 0° C.–5° C. an additional 2 hours while monitoring by TLC (20% ethyl acetate/hexane, UV). The reaction is then allowed to warm to room temperature, filtered and the filtrate concentrated. The residue is dissolved in diethyl ether/ethyl acetate (500 ml/250 ml) and washed with H2O, 2.5 N HCl, aqueous NaHCO3, brine, dried (Na2SO4), filtered, concentrated, and triturated with petroleum ether to give 126 g of 2-bromo-4,6-difluoro-N-carbethoxy aniline (94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087635B2
Source datasetuspto-grants-2006_08
ORD IDord-71909e61d7c54e33a7c5b60a56e3b72e
Source noteuspto-grants-2006_08