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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198080Generated: October 30, 2026

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

https://huagongshe.com/reaction/2198080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductPhenyl [5-(trifluoromethyl)pyridin-2-yl]carbamateHCID 1142604269%

Reaction Steps

A solution of 5-(trifluoromethyl)pyridin-2-amine (100 mg, 0.617 mmol) and N,N-diisopropylethylamine (159.5 mg, 215 μL, 1.234 mmol) in 5 mL CH2Cl2 was treated with phenyl chloroformate (106 mg, 85 μL, 0.68 mmol) and left to stir for 3 h at rt. Solution was diluted with EtOAc and washed twice with 1 N HCl and 1 time with brine. The organic layer was dried (Na2SO4) and concentrated to provide a white solid. Tituration with 10% EtOAc in hexanes gave 120 mg (69%, 0.42 mmol) of the above compound as a white solid. 1H-NMR (DMSO-d6) δ 11.26 (s, 1H), 8.70 (s, 1H), 8.22 to 8.16 (m, 1H), 7.99 (d, J=8 Hz, 1H), 7.45 to 7.40 (m, 2H), 7.30 to 7.20 (m, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338595B2
Source datasetuspto-grants-2012_12
ORD IDord-cd3d9c43091548c3a9f4bc92ac3afde5
Source noteuspto-grants-2012_12