HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexyl isocyanate → O-[3-(2,2-dimethoxyethylthio) phenyl] N-cyclohexylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexyl isocyanate | HCID 18502 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | 3-(2,2-Dimethoxyethylthio)phenol | HCID 20396673 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | O-[3-(2,2-dimethoxyethylthio) phenyl] N-cyclohexylcarbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04163112 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-7a220c07b4134e0d8af9adf6ac663986 |
| Source note | uspto-grants-1979_07 |