HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylamine → Dicyclohexylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylamine | HCID 7582 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22826593 | HCID 22826593 | — |
| Reactant | HCID 86739430 | HCID 86739430 | — |
| Solvent | Water | HCID 962 | — |
| Product | Dicyclohexylamine | HCID 7582 | — |
| Product | HCID 12893584 | HCID 12893584 | — |
Reaction Steps
A solution of 1.4 g of potassium carbonate in 30 ml of water is added to 2.8 g of 3-(3-bromo-2-methylpropionyl)-4(R)-thiazolidinecarboxylic acid whereupon 3 g of potassium 4-chloro-3-sulfamoyl-thiobenzoate is added slowly under ice-cooling and stirring, and the resulting mixture is stirred at room temperature for 4 hours. The reaction mixture is then treated in an analogous manner of Example 1, and the oily residue thus obtained is converted in a conventional manner into the dicyclohexylamine salt. Thus is obtained dicyclohexylamine salt of 3-[3-(4-chloro-3-sulfamoylbenzoylthio)-2(S)-methylpropionyl]-4(R)-thiazolidinecarboxylic acid as white crystalline powder, melting at 173°-176° C. (recrystallized twice from isopropanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04450275 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-85874b7c453b476f95a6972907cd04f2 |
| Source note | uspto-grants-1984_05 |