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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707161Generated: October 29, 2026

Pyridine → Phenyl 4-carbamoylphenylcarbamate

https://huagongshe.com/reaction/707161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPentaneHCID 8003—
ReactantPhenyl chloroformateHCID 15891—
Reactant4-AminobenzamideHCID 76079—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductPhenyl 4-carbamoylphenylcarbamateHCID 6063122977%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 4-aminobenzamide (5.0 g, 36.7 mmol) and pyridine (2.9 g, 36.7 mmol)) in dry CH2Cl2 (100 mL) at −10° C., phenyl chloroformate (6.9 g, 44.1 mmol) was added dropwise, stirred at −10° C. for 30 min and then at room temperature for 30 minutes The reaction mixture was diluted with CH2Cl2 (100 mL) and washed with water (2×70 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated to get the crude product. The crude product was dissolved in diethyl ether (15 mL) and sonicated for 10 minutes and then pentane (30 mL) was added, the resulting solid was filtered and washed with pentane to give phenyl 4-carbamoylphenylcarbamate (7.2 g, 77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174963B2
Source datasetuspto-grants-2015_11
ORD IDord-45fbb770fc1e47f99baf5342982a41e4
Source noteuspto-grants-2015_11