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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731425Generated: October 25, 2026

Iodine → Methyl phenylcarbamate

https://huagongshe.com/reaction/1731425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantNitrobenzeneHCID 7416—
ReactantCarbanilideHCID 7595—
ReactantTriethylamineHCID 8471—
ReactantHCID 178418416HCID 178418416—
CatalystPotassiumHCID 5462222—
SolventMethanolHCID 887—
ProductMethyl phenylcarbamateHCID 17451—

Reaction Steps

In a 200 ml stirring type autoclave were charged 30 mmols of N,N'-diphenylurea, 15 mmols of nitrobenzene, 50 ml of methanol, 1 mmol of potassium tetrabromopalladate, 2 mmols of iodine and 2 mmols of triethylamine. 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 6 hours with stirring. As the result of analysis of the reaction solution, the conversions of N,N'-diphenylurea and nitrobenzene were 30% and 38%, respectively, and 15 mmols of methyl N-phenylcarbamate were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04621149
Source datasetuspto-grants-1986_11
ORD IDord-de11fa3b8cac42f689442ceea5846ca8
Source noteuspto-grants-1986_11