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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489370Generated: October 30, 2026

2-Chlorobenzaldehyde → HCID 178439374, compound

https://huagongshe.com/reaction/489370

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactant3-OxohexanenitrileHCID 9793723—
ReactantHCID 178418806HCID 178418806—
SolventAcetonitrileHCID 6342—
ProductHCID 178439374HCID 17843937436.2%

Reaction Steps

To a solution of acetonitrile (4.8 g) in THF (150 mL) was added n-BuLi (67 mmol) at −78° C. Further, methyl butanoate (10 g) was added and the mixture was stirred for one hour. After acidification with hydrochloric acid, the mixture was extracted with ethyl acetate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate (10:1)) to give 1-cyanopentan-2-one (5.5 g) as a colorless oil. A solution of 2-chlorobenzaldehyde (1.9 g), 3-aminopyrazole (1.0 g) and 1-cyanopentan-2-one (1.6 g) in acetonitrile (20 mL) was heated under reflux overnight. The reaction mixture was cooled to room temperature, and the precipitated crystals were collected by filtration to give the title compound (1.3 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977262B2
Source datasetuspto-grants-2005_12
ORD IDord-7ae107ef36c34414a3255deee1d15a25
Source noteuspto-grants-2005_12