Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 23289168 | HCID 23289168 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 23289163 | HCID 23289163 | 75% |
Reaction Steps
0.50 g (1.2 mmol) of 3-(4-chloro-3-cyanomethyl-6-fluoro-2-methylbenzofuran-7-yl)-1-methyl-6-trifluoromethyluracil was dissolved in 30 ml of 50% sulfuric acid, followed by stirring at 60° C. for 2 hours. After completion of the reaction, the reaction solution was poured into water and extracted with ethyl acetate. The organic layer was washed sequentially with water and a saturated sodium chloride aqueous solution and then, dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. Then, the obtained residue was purified by silica gel column chromatography to obtain 0.39 g (yield: 75%) of the desired product as white crystals. Melting point: 127-129° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06130187 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-da518ba120114cdcbd772d0b7e42451a |
|---|
| Source note | uspto-grants-2000_10 |
|---|