HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-Phenoxy-1-phenyl-1H-pyrazolo[3,4-b]pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Chloro-1-phenyl-1H-pyrazolo[3,4-b]pyrazine | HCID 13271936 | — |
| Solvent | Phenol | HCID 996 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Phenoxy-1-phenyl-1H-pyrazolo[3,4-b]pyrazine | HCID 13271948 | 92% |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
In 5.0 (0.053 mole) of phenol was dissolved 0.34 g (0.0085 mole) of sodium hydroxide, and 1.00 g (0.0043 mole) of 5-chloro-1-phenyl-1H-pyrazolo[3,4-b]pyrazine was added to the solution. The mixture was maintained at 150° C. for 2 hours. The reaction mixture was dissolved in chloroform, and the resulting solution was washed with an aqueous 10% solution of sodium hydroxide and then dried. The solvent was removed by distillation, and the residue was recrystallized from a benzene-hexane mixed solvent to obtain 1.20 g (the yield was 92%) of 5-phenoxy-1-phenyl-1H-pyrazolo[3,4-b]pyrazine in the form of a colorless needle crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04460773 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-504a491dcdc5474a846959c9eb60f325 |
| Source note | uspto-grants-1984_07 |