HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 136109128, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | 3-Bromo-4-fluorobenzaldehyde | HCID 173604 | — |
| Reactant | HCID 178418806 | HCID 178418806 | — |
| Product | HCID 136109128 | HCID 136109128 | 49% |
Reaction Steps
A solution of 1,3-cyclohexanedione(0.56 g, 5 mmol), 3-bromo-4-fluorobenzaldehyde(1.01 g, 5 mmol), and 3-aminopyrazole (0.41 g, 5 mmol) in ethanol (5 mL) was heated at reflux for 24 hours. After the reaction mixture was allowed to cool to ambient temperature, the volatiles were evaporated at reduced pressure and the resulting residue was chromatographed on silica gel, eluting with 5% ethanol/methylene chloride to provide 0.9 g (49 %) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06274587B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-5ed99fe157df44c4a0a543f900c29c14 |
| Source note | uspto-grants-2001_08 |