HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → N-(2,6-Diethyl-phenyl)-N'-tert.-butyl-thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | Calcium Carbonate | HCID 10112 | — |
| Reactant | 2,6-Diethylaniline | HCID 11369 | — |
| Reactant | 2,6-Diethylphenyl isothiocyanate | HCID 141193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2,6-Diethyl-phenyl)-N'-tert.-butyl-thiourea | HCID 20346927 | — |
Reaction Steps
2,6-Diethyl-phenyl isothiocyanate can be prepared as follows: 100 g of 2,6-diethylaniline in 200 ml of methylene chloride are added dropwise at 0°-5°, whilst stirring, to a mixture of 500 ml of methylene chloride, 300 ml of water, 120 g of calcium carbonate and 92 g of thiophosgene. The mixture is then heated to the reflux temperature until the evolution of CO2 has ended. The cooled batch is filtered and the methylene chloride layer is separated off, dried with calcium chloride and fractionated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04194008 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-f9f97215daf94e67ae5df4197d44dfa3 |
| Source note | uspto-grants-1980_03 |