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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528036Generated: October 27, 2026

2',4',6'-Trihydroxyacetophenone → 1-[2,4,6-Trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone

https://huagongshe.com/reaction/1528036

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2',4',6'-TrihydroxyacetophenoneHCID 68073—
Reactant4-Bromo-2-methylbut-1-eneHCID 549585—
SolventPotassium HydroxideHCID 14797—
Product1-[2,4,6-Trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanoneHCID 1097962738.7%

Reaction Steps

1-(2,4,6-trihydroxyphenyl]ethanone (2.0 mg, 11.9 mmol) was dissolved in a 5% potassium hydroxide aqueous solution (20 mL). After the mixture was cooled below 0° C., isopentenyl bromide (3.6 g, 24 mmol) was slowly added dropwise within 30 min. The reaction mixture was stirred at room temperature for 2 hours, then poured into an ice water and acidified to pH 2. The reaction mixture was extracted with ethyl acetate. The extract was collected and dried over anhydrous sodium sulfate. After removal of the solvent, the residue was purified by silica gel column chromatography (dichloromethane as eluent) to give the desired compound (0.7 g, yield 20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090583B2
Source datasetuspto-grants-2015_07
ORD IDord-3cb7b15b61034ec69b25282892b2f98a
Source noteuspto-grants-2015_07