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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650515Generated: October 30, 2026

Ethanol → HCID 136109128, compound

https://huagongshe.com/reaction/650515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1,3-CyclohexanedioneHCID 10434—
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
ReactantHCID 178418806HCID 178418806—
ProductHCID 136109128HCID 13610912849%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274587B1
Source datasetuspto-grants-2001_08
ORD IDord-5ed99fe157df44c4a0a543f900c29c14
Source noteuspto-grants-2001_08