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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862357Generated: November 2, 2026

Ethanol → HCID 136109128, compound

https://huagongshe.com/reaction/1862357

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 numberUS06538000B1
Source datasetuspto-grants-2003_03
ORD IDord-58ee717588ac4981b78cfb3fdf7464bd
Source noteuspto-grants-2003_03