HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrafluorophthalic anhydride → 5-Ethyl-1-phenyl-5-(tetrafluorophthalimido)barbituric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrafluorophthalic anhydride | HCID 69545 | — |
| Reactant | 5-Amino-5-ethyl-1-phenylbarbituric acid | HCID 15424937 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Ethyl-1-phenyl-5-(tetrafluorophthalimido)barbituric acid | HCID 9933393 | 60.1% |
Reaction Steps
A mixture of about 250 mg (about 1 mmol) of 5-amino-5-ethyl-1-phenylbarbituric acid, about 260 mg (about 1.2 mmol) of tetrafluorophthalic anhydride, and about 7 mL of acetic acid was refluxed for about 3 hours. The solvent was evaporated to dryness under reduced pressure of from about 200 to about 15 mbar. The residue was recrystallized from ethyl alcohol to yield about 270 mg 5-ethyl-1-phenyl-5-(tetrafluorophthalimido)barbituric acid (a 60% yield) having a melting point of about 218° to about 220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716315B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-7d018a947d9a44d59d443296a3e00f66 |
| Source note | uspto-grants-2014_05 |