HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 24765764, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tetrafluorophthalic anhydride | HCID 69545 | — |
| Reactant | HCID 66811031 | HCID 66811031 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 24765764 | HCID 24765764 | — |
Reaction Steps
A mixture of 5-amino-1,5-dimethylbarbituric acid hydrochloride (0.31 g, 1.50 mmol), tetrafluorophthalic anhydride (0.40 g, 1.80 mmol) and Et3N (0.21 mL, 0.15 g, 1.50 mmol) in glacial AcOH (11 mL) was stirred under reflux for 3 hours. The yellow solution was then allowed to cool down to room temperature and evaporated to dryness under reduced pressure. The oily residue was recrystallized from 70% EtOH to give 1,5-dimethyl-5-(tetrafluorophthalimido)-barbituric acid (19a) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143252B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-32217543272b4ae0b99ce0d8fec53094 |
| Source note | uspto-grants-2012_03 |