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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731422Generated: November 1, 2026

Ethanol → Ethyl N-phenylcarbamate

https://huagongshe.com/reaction/1731422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAnilineHCID 6115—
ReactantNitrobenzeneHCID 7416—
ReactantCarbon tetraiodideHCID 10487—
ReactantRubidium hydroxideHCID 62393—
ReactantHCID 178418416HCID 178418416—
CatalystPalladium ChlorideHCID 24290—
ProductEthyl N-phenylcarbamateHCID 7591—

Reaction Steps

In a 200 ml stirring type autoclave were charged 30 mmols of aniline, 15 mmols of nitrobenzene, 50 ml of ethanol, 3 mmols of palladium chloride, 3 mmols of tetraiodomethane and 3 mmols of rubidium hydroxide. After the air inside the autoclave had been replaced with carbon monoxide, carbon monoxide was pressurized into the autoclave to 120 Kg/cm2, and the reaction was carried out at 180° C. for 5 hours with stirring. As the result of analysis of the reaction solution, the conversions of aniline and nitrobenzene were 21% and 29%, respectively, and 8 mmols of ethyl N-phenylcarbamate were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04621149
Source datasetuspto-grants-1986_11
ORD IDord-fa798d41ff08449c9a5db5ad96fd995c
Source noteuspto-grants-1986_11