HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloride → HCID 178514107, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | HCID 178418790 | HCID 178418790 | — |
| Reactant | HCID 178513210 | HCID 178513210 | — |
| Reactant | HCID 178513445 | HCID 178513445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178514107 | HCID 178514107 | — |
| Product | HCID 178514168 | HCID 178514168 | — |
Reaction Steps
In equation (1) the pseudourea of 2-thiopseudourea is liberated from its corresponding chloride or sulfate salt with an equivalent amount of sodium hydroxide in a mixture of water and dichloromethane at 0° to 5°C. The isocyanate or isothiocyanate is then added and after stirring for 1 to 24 hours at room temperature the organic layer is separated, dried, and the solvent removed by evaporation to give the intermediate allophanimidate, thioallophanimidate, or dithioallophanimidate ester (This reaction is essentially the same as described in Organic Synthesis, 42, 87, for the preparation of methyl 4-phenyl-3-thioallophanimidate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03954837 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-5b65664f2b904eac969eac3fc683ea42 |
| Source note | uspto-grants-1976_05 |