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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427610Generated: October 30, 2026

2-Methoxy-5-nitroaniline → Carbamic acid, (2-methoxy-5-nitrophenyl)-, phenylmethyl ester

https://huagongshe.com/reaction/427610

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-5-nitroanilineHCID 7447—
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductCarbamic acid, (2-methoxy-5-nitrophenyl)-, phenylmethyl esterHCID 493566286%

Reaction Steps

To a stirred solution of 2-methoxy-5-nitroaniline (5.0 g, 30 mmol) and potassium carbonate (12 g, 90 mmol) in tetrahydrofuran (200 mL) and water (100 mL) was added benzyl chloroformate (6.1 g, 36 mmol). After 12 h, the mixture was diluted with ethyl acetate (200 mL) and the layers were separated. The organic phase was washed twice with 1 N aqueous hydrochloric acid, once with saturated aqueous sodium chloride solution, twice with saturated aqueous sodium bicarbonate solution, twice with saturated aqueous sodium chloride solution, dried (magnesium sulfate), filtered, and concentrated in vacuo. The resulting solid was suspended in diethyl ether and after sonication, the solid was filtered, washed with diethyl ether, and dried in vacuo to give 7.8 g (86%) of the title compound as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313122B1
Source datasetuspto-grants-2001_11
ORD IDord-1e055435ee044e48a75ca3c72af4c6a7
Source noteuspto-grants-2001_11