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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566194Generated: November 1, 2026

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

https://huagongshe.com/reaction/566194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
Reactant5-Allyloxy-4-bromo-2-fluoroanilineHCID 21265598—
SolventDichloromethaneHCID 6344—
Productethyl N-(5-allyloxy-4-bromo-2-fluorophenyl)carbamateHCID 2126555998.5%

Reaction Conditions

Temperature10 °C

Reaction Steps

Ethyl chloroformate (5.97 g) was added dropwise to a solution of 5-allyloxy-4-bromo-2-fluoroaniline (12.3 g) and pyridine (7.90 g) in methylene chloride (100 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 to obtain to the objective ethyl N-(5-allyloxy-4-bromo-2-fluorophenyl)carbamate (15.67 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174839B1
Source datasetuspto-grants-2001_01
ORD IDord-fc87c21c7daf4bdfac9311e38a6a25ec
Source noteuspto-grants-2001_01