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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782114Generated: November 3, 2026

2',4'-Dihydroxyacetophenone → HCID 23110664, compound

https://huagongshe.com/reaction/1782114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2',4'-DihydroxyacetophenoneHCID 6990—
ReactantHCID 521026HCID 521026—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventPotassium hydroxide methanolHCID 23689386—
ProductHCID 23110664HCID 23110664—

Reaction Steps

2′,4′-Dihydroxyacetophenone (manufactured by Wako Pure Chemical Industries, Ltd.) was treated with 1-bromo-2-methyl-2-butene (manufactured by Aldrich) in 2 M KOH/methanol solution under ice-cooling, and thereafter the treated solution was hydrogenated in methanol, in the presence of palladium black (manufactured by Nakalai Tesque, Inc.), to give 2′,4′-dihydroxy-3′-(3-methylbutyl)acetophenone. Subsequently, 2′,4′-dihydroxy-3′-(3-methylbutyl)acetophenone and 4-hydroxybenzaldehyde (manufactured by Aldrich) were subjected to Claisen condensation, to give a yellow substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498357B2
Source datasetuspto-grants-2009_03
ORD IDord-01f836b342f54dd0904850f3d1fe6486
Source noteuspto-grants-2009_03