HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthaldehyde → HCID 135482176, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthaldehyde | HCID 6195 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | HCID 178418806 | HCID 178418806 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 135482176 | HCID 135482176 | 44.4% |
Reaction Steps
A solution of 1,3-cyclohexanedione (0.11 g, 1 mmol), 1-naphthaldehyde (0.16 g, 1 mmol), and 3-aminopyrazole (0.11 g, 1.27 mmol) in ethanol (10 mL) were heated at 80° C. in a sealed 20 mL vial for 3 days. After the reaction mixture was allowed to cool to ambient temperature, the solvent was evaporated at reduced pressure and the resulting residue was chromatographed on silica gel, eluting with 5% ethanol/methylene chloride to provide 0.14 g (44%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06538000B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-00fcf70a13d4438ba0b171157f7feea6 |
| Source note | uspto-grants-2003_03 |