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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413260Generated: November 1, 2026

Phenyl chloroformate → Phenyl [5-(trifluoromethyl)pyridin-2-yl]carbamate

https://huagongshe.com/reaction/413260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
Reactant2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
ReactantEthyl acetate hexaneHCID 21226206—
SolventPyridineHCID 1049—
ProductPhenyl [5-(trifluoromethyl)pyridin-2-yl]carbamateHCID 11426042—

Reaction Steps

Dissolve 2-amino-5-trifluoromethylpyridine (162 mg, 1.0 mmole) in pyridine (2.0 mL) under nitrogen at room temperature. Add drop wise phenyl chloroformate (0.125 mL, 1.0 mmole) to the reaction mixture at room temperature. Stir the mixture for 24 hours and new spot is noticed in TLC (30% EtOAc/hexane). Evaporate the reaction mixture under vacuo and purify the crude by flash column chromatography on a silica gel using CHCl3 to afford (5-Trifluoromethyl-pyridin-2-yl)-carbamic acid phenyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566367B2
Source datasetuspto-grants-2003_05
ORD IDord-3f4c076a7bf44596876ee5ff49ceba89
Source noteuspto-grants-2003_05