Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 20432881 | HCID 20432881 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15583091 | HCID 15583091 | — |
Reaction Steps
13.2 g (0.077 mole) butyric acid-N-(1,2,3-thiadiazole-5-yl)-amide were dissolved in 150 ml absolute tetrahydrofuran and reacted with 3.36 g (0.077 mole) of a 55% dispersion of sodium hydride in oil, whereby during the addition the reaction solution through cooling is maintained at 30° C. After about 30 minutes of stirring at room temperature, the evolution of hydrogen is completed. 8.3 ml (0.077 mole) phenylisocyanate is added dropwise within about 5 minutes during which time the reaction temperature increases to 36° C. The reaction mixture is then stirred at room temperature for 1.5 hours whereby a thick crystaline slurry is formed. The reaction mixture is then introduced into a solution of 12.3 ml (0.154 mole) concentrated hydrochloric acid in 300 ml of water. Thereafter the reaction mixture is extracted with 250 ml acetic ester, the organic phase washed with water, dried over magnesium sulfate, filtered and concentrated in vacuum. There were thusly obtained colorless crystals which were digested with 50 ml diisopropylether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04491466 |
|---|
| Source dataset | uspto-grants-1985_01 |
|---|
| ORD ID | ord-4d48a4527a3b4461b532883a37974ec6 |
|---|
| Source note | uspto-grants-1985_01 |
|---|