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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726332Generated: October 30, 2026

Pyridine → 4-Dimethylaminocyclohexanone 4-bromophenylhydrazone

https://huagongshe.com/reaction/726332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromophenylhydrazine hydrochlorideHCID 12157—
Reactant4-(Dimethylamino)cyclohexan-1-oneHCID 10374545—
SolventEthanolHCID 702—
Product4-Dimethylaminocyclohexanone 4-bromophenylhydrazoneHCID 2261148987%

Reaction Steps

To a mixture of 6.0 gm (42.0 mMol) 4-dimethylaminocyclohexanone and 9.5 gm (42.0 mMol) 4-bromophenylhydrazine hydrochloride in 100 mL ethanol were added 3.4 mL (42 mMol) pyridine. The resultant mixture was then heated at reflux for 2 hours and then stirred at ambient temperature for 18 hours. The reaction mixture was then treated with aqueous potassium carbonate and extracted well with dichloromethane. The organic phases were combined, dried over sodium sulfate and concentrated under reduced pressure. The resultant residue was treated with toluene and concentrated again under reduced pressure to give 11.3 gm (87%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05708187
Source datasetuspto-grants-1998_01
ORD IDord-761fa6a935da4198888316d4862f2564
Source noteuspto-grants-1998_01