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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513480Generated: October 28, 2026

Pyridine → Phenyl 4-carbamoylphenylcarbamate

https://huagongshe.com/reaction/1513480

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 numberUS08217036B2
Source datasetuspto-grants-2012_07
ORD IDord-1e3a6e16bf794ebca52e7f88f7005fb7
Source noteuspto-grants-2012_07