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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566184Generated: November 2, 2026

Pyridine → ethyl N-(4-bromo-5-ethoxy-2-fluorophenyl)carbamate

https://huagongshe.com/reaction/566184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
Reactant4-Bromo-5-ethoxy-2-fluoroanilineHCID 13281429—
SolventDichloromethaneHCID 6344—
Productethyl N-(4-bromo-5-ethoxy-2-fluorophenyl)carbamateHCID 2126558896.3%

Reaction Conditions

Temperature10 °C

Reaction Steps

Ethyl chloroformate (2.15 g) was added dropwise to a solution of 4-bromo-5-ethoxy-2-fluoroaniline (4.21 g) and pyridine (2.84 g) in methylene chloride (36 ml) at 0° C., and the mixture was stirred at 10° C. for 3 hours. After the reaction, this was extracted with methylene chloride, then washed with diluted hydrochloric acid and an aqueous sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate. Then, methylene chloride was distilled off, and the resulting crude crystals were crystallized from a mixed solvent of ethyl acetate and n-hexane (1:5 v/v) to obtain the objective ethyl N-(4-bromo-5-ethoxy-2-fluorophenyl)carbamate (5.30 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174839B1
Source datasetuspto-grants-2001_01
ORD IDord-296db66172274adf93bcc36a6c01abf3
Source noteuspto-grants-2001_01