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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972127Generated: November 1, 2026

Cyclohexyl isocyanate → O-[3-(2,2-dimethoxyethylthio) phenyl] N-cyclohexylcarbamate

https://huagongshe.com/reaction/972127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl isocyanateHCID 18502—
ReactantIsocyanateHCID 105034—
Reactant3-(2,2-Dimethoxyethylthio)phenolHCID 20396673—
CatalystTriethylamineHCID 8471—
SolventBenzeneHCID 241—
ProductO-[3-(2,2-dimethoxyethylthio) phenyl] N-cyclohexylcarbamateHCID 20396715—

Reaction Steps

3-(2,2-Dimethoxyethylthio)phenol (0.05 mole) dissolved in benzene (10 ml) is charged into a glass reaction flask equipped with a mechanical stirrer. Cyclohexyl isocyanate (0.06 mole) and triethylamine (3 drops) are then added, and the resulting mixture is stirred at room temperature for a period of about 6 hours. The mixture is then stripped of solvent and unreacted isocyanate to yield the desired product O-[3-(2,2-dimethoxyethylthio) phenyl] N-cyclohexylcarbamate as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04163112
Source datasetuspto-grants-1979_07
ORD IDord-7a220c07b4134e0d8af9adf6ac663986
Source noteuspto-grants-1979_07