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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408682Generated: October 30, 2026

4-Methylcyclohexanone → 6-Bromo-4'-methylspiro(chroman-2,1'-cyclohexan)-4-one

https://huagongshe.com/reaction/1408682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylcyclohexanoneHCID 11525—
ReactantPyrrolidineHCID 31268—
Reactant5'-Bromo-2'-hydroxyacetophenoneHCID 95991—
SolventMethanolHCID 887—
Product6-Bromo-4'-methylspiro(chroman-2,1'-cyclohexan)-4-oneHCID 58424034156.5%

Reaction Steps

A mixture of 1-(5-bromo-2-hydroxy-phenyl)-ethanone (20 g, 0.093 mol), 4-methylcyclohexanone (21.31 g, 0.187 mol) and pyrrolidine (12.63 g, 0.178 mol) in methanol (400 mL) was refluxed for overnight. The reaction mixture was concentrated in vacuo, diluted with an equal volume of H2O and then added HCl until pH=1. The resulting mixture was extracted with EtOAc. The organic layer was dried over anhydrous Na2SO4, filtered, and evaporated to give 6-bromo-4′-methylspiro(chroman-2,1′-cyclohexan)-4-one (45 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921359B2
Source datasetuspto-grants-2014_12
ORD IDord-a507d3fd2ed142aebdd4c7b56d6c9d5b
Source noteuspto-grants-2014_12