Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | HCID 13369979 | HCID 13369979 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178513105 | HCID 178513105 | — |
Reaction Steps
Guanidine hydrochloride (7.8 g) is suspended in acetone (150 ml). A 50% aqueous sodium hydroxide solution (6.53 g) is added to the guanidine suspension. The mixture is stirred for one and one-half hours, after which 15 g anhydrous sodium sulfate are added and the reaction mixture stirred vigorously for an additional hour. The isocyanate obtained in Step 5 above (8.0 g) is dissolved and suspended in 50 ml acetone. This suspension is added to the reaction mixture over a period of one hour fifteen minutes. The reaction mixture is stirred overnight, filtered, and the filtrate evaporated in vacuo to a green oil. The green oil is triturated in 200 ml of H2O containing 5 drops of a 50% aqueous sodium hydroxide solution. The resulting suspension is stirred for three hours, filtered, and the solid washed with water and dried. After air drying overnight, there is obtained 12.9 g of a white powder which is dried in vacuo at 30°-35° C. for four hours, giving 9.47 g of white powder. The powder is dissolved in 50 ml of methanol. The methanol solution is filtered and the filtrate acidified with methanol/HCl. The acidified solution is evaporated in vacuo (30°-35° C.) to yield the hydrochloride salt as a light-colored oil, which is utilized without further treatment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04487779 |
|---|
| Source dataset | uspto-grants-1984_12 |
|---|
| ORD ID | ord-e0c5d84f6f374fbea1af4dfc6d1cb79e |
|---|
| Source note | uspto-grants-1984_12 |
|---|