HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → HCID 49817597, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Methyl 3-oxo-4-(2,4,5-trifluorophenyl)butanoate | HCID 29942605 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 49817597 | HCID 49817597 | — |
Reaction Steps
Methyl 4-(2,4,5-trifluorophenyl)acetoacetate (21) was treated with anhydrous ammonium acetate in an alcoholic solvent, preferably methanol, and preferably at higher temperature, preferably at 60-65° C. The methyl(Z)-3-amino-4-(2,4,5-trifluorophenyl)but-2-enoate (28) formed was preferably isolated by complete removal of the solvent under reduced pressure, separation of excess of ammonium acetate by using a polar organic solvent such as ethyl acetate, distillation of the polar organic solvent and triturating the product with non-polar solvents like hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846916B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-b69e673b0ef143fe8944eb5b352bf358 |
| Source note | uspto-grants-2014_09 |