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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786101Generated: October 31, 2026

Ethyl chloroformate → Ethyl (4-bromo-2-cyanophenyl)carbamate

https://huagongshe.com/reaction/1786101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant2-Amino-5-bromobenzonitrileHCID 429740—
ProductEthyl (4-bromo-2-cyanophenyl)carbamateHCID 1836785768%

Reaction Steps

A suspension of 2-amino-5-bromobenzonitrile (58.5 g, 297 mmol) in ethyl chloroformate (141 mL, 1.48 mol) was heated at reflux for 5 h. The excess ethyl chloroformate (99 mL) was distilled off and toluene (96 mL) was added. Slow addition of cyclohexane (228 mL) induced crystallization. The resulting solid was collected by filtration and rinsed with cyclohexane. Drying in vacuo afforded the title compound (54.3 g, 68%) as an orange solid. MS: m/e=267.1/269.2 [M—H−].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507728B2
Source datasetuspto-grants-2009_03
ORD IDord-c226dfd0b3a249e6993d3cfb1ff6271d
Source noteuspto-grants-2009_03