HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 18317684, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Hydrazinium chloride | HCID 115031 | — |
| Reactant | 5-(2-Chlorophenyl)cyclohexane-1,3-dione | HCID 875360 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18317684 | HCID 18317684 | 4.1% |
Reaction Steps
A solution of 5-(2-chlorophenyl)-cyclohexane-1,3-dione (1.0 g), hydrazine hydrochloride (0.31 g) in ethanol (10 ml) was refluxed for 3 hours. To the solution was added benzaldehyde (1.5 g), and the mixture was refluxed for 4 days. Under reduced pressure, the solvent was evaporated, and the residue was purified with silica gel column chromatography to give crystals, which were recrystallized from ethyl acetate-hexane to give 6-(2-chlorophenyl)-3-phenyl-4,5,6,7-tetrahydroindazol-4-one (0.06 g) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06350749B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-f2e98b90d6384cbbb77a8c82acd22144 |
| Source note | uspto-grants-2002_02 |