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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427253Generated: October 27, 2026

Citric Acid → methyl N-[1-(3-bromophenyl)ethyl]carbamate

https://huagongshe.com/reaction/427253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantPyridineHCID 1049—
ReactantMethyl chloroformateHCID 6586—
Reactant1-(3-Bromophenyl)ethanamineHCID 16785764—
SolventTolueneHCID 1140—
Productmethyl N-[1-(3-bromophenyl)ethyl]carbamateHCID 1548379234.2%

Reaction Steps

To a solution of 23.8 g of 3-bromo-α-methylbenzylamine in toluene (120 ml), 14.1 g of pyridine was added at room temperature. To this solution, 18.6 g of methyl chloroformate was dropwise added under cooling with ice, followed by stirring at room temperature for 2 hours. The reaction solution was poured into a citric acid aqueous solution and extracted with ethyl acetate. The organic layer was washed with a citric acid aqueous solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 10.5 g of methyl N-[1-(3-bromophenyl)ethyl]carbamate as a colorless transparent viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313071B1
Source datasetuspto-grants-2001_11
ORD IDord-f9f3808b31a5484d9c9deeeb7c97155d
Source noteuspto-grants-2001_11