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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496278Generated: October 31, 2026

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

https://huagongshe.com/reaction/496278

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. B. 1′-(5-Trifluoromethyl-pyridin-2-yl-carbamoyl)spiroisobenzofuran-1,4′-piperidine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943199B2
Source datasetuspto-grants-2005_09
ORD IDord-3f2820510d04447289709e6f976b251e
Source noteuspto-grants-2005_09