HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → HCID 68677556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 68675630 | HCID 68675630 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68677556 | HCID 68677556 | — |
Reaction Steps
A solution of 8.60 g of the product of Step C and 21.30 g of ammonium acetate in MeOH was heated in a sealed system at 100° C. for 24 h. The solution was cooled to ambient temperature and concentrated to leave an oil that was partitioned between EtOAc and water. The aqueous layer was acidified to pH 5 with concentrated HCl and then extracted with EtOAc. The combined organic layers were washed with sat. sodium chloride, dried over sodium sulfate, filtered, and concentrated to provide 2,6-di-tert-butyl-2H,7H-[1,2,4]triazolo[4,3-a]pyrazine-3,8-dione as a white solid. MS (M+H+)=265.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709473B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-256a1cf901e64a268c09b48ce576c220 |
| Source note | uspto-grants-2010_05 |