Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyurea | HCID 3657 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,4-Heptanedione, 6-methyl- | HCID 76354 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178425012 | HCID 178425012 | 58% |
Reaction Steps
0.20 mol (15.21 g) hydroxy urea were dissolved in 300 ml of M HCl, 300 ml of methanol were added, and 0.20 mol (28.44 g) 6-methyl-2,4-heptanedione were added dropwise while cooling at −12 to −10° C. The solution was allowed to warm slowly to room temperature and stirred over night, then evaporated to dryness. The residue was suspended with 200 ml of acetone, the mixture cooled to below 0° C. in an ice/ethanol bath, the solid filtered off and washed with a little ice-cold acetone. After drying 7.23 g of a product was obtained, which contained 58% of the title compound and 42% of the by-product ammonium chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09422247B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-7a2e6175695c4873bd703fc7e5ba2b7d |
|---|
| Source note | uspto-grants-2016_08 |
|---|