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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180516Generated: November 3, 2026

2-[(Dimethylamino)methylidene]cyclohexane-1,3-dione → 1-(3,4-dichlorophenyl)-1,5,6,7-tetrahydro-4H-indazol-4-one

https://huagongshe.com/reaction/1180516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[(Dimethylamino)methylidene]cyclohexane-1,3-dioneHCID 359353—
ReactantSodium AcetateHCID 517045—
Reactant(3,4-Dichlorophenyl)hydrazine monohydrochlorideHCID 3084323—
SolventAcetic AcidHCID 176—
Solvent1-ButanolHCID 263—
Product1-(3,4-dichlorophenyl)-1,5,6,7-tetrahydro-4H-indazol-4-oneHCID 2311290456%

Reaction Steps

A mixture of 1-(3,4-dichlorophenyl)hydrazine hydrochloride (6.78 g, 31.8 mmol) and anhydrous sodium acetate (2.60 g, 31.8 mmol) in n-BuOH (20 mL) is slowly added to a solution of 2-((dimethylamino)methylene)cyclohexane-1,3-dione (5.32 g, 31.8 mmol) in n-BuOH (100 mL) and acetic acid (5 mL). The resulting mixture is heated to reflux during 2 hours, effecting follow-up of the reaction by TLC. The solvent is evaporated at reduced pressure, the residue is diluted in AcOEt and washed with H2O. The solvent is next evaporated, and the crude is purified by silica-gel chromatography, to obtain 1-(3,4-dichlorophenyl)-1,5,6,7-tetrahydro-4H-indazol-4-one (5.0 g, 17.79 mmol, 56%, orange solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282499B2
Source datasetuspto-grants-2007_10
ORD IDord-c7061717fc1541cc856fd8bb0e9c9424
Source noteuspto-grants-2007_10