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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030680Generated: October 25, 2026

1-Chloro-3-methyl-2-butene → Ethanone, 1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl]-

https://huagongshe.com/reaction/1030680

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-3-methyl-2-buteneHCID 10429—
ReactantPotassium CarbonateHCID 11430—
Reactant2',4',6'-TrihydroxyacetophenoneHCID 68073—
SolventTetrahydrofuranHCID 8028—
ProductEthanone, 1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl]-HCID 1168731155%

Reaction Steps

In 250 ml of anhydrous tetrahydrofuran was dissolved 50.0 g of 2',4',6'-trihydroxyacetophenone, and 123.1 g of anhydrous potassium carbonate was added to the solution and the mixture was stirred at room temperature for 30 minutes. Then, 37.2 g of 1-chloro3-methyl-2-butene was added dropwise to the mixture over a period of 20 minutes and reaction was carried out at room temperature for 24 hours. After the reaction, the reaction mixture was extracted with 2 l of ethyl acetate and the solvent was removed from the ethyl acetate layer by distillation, and the residue was recrystallized from a benzene/petroleum ether mixed solvent to obtain 38.6 g (yield=55.0%) of 2',4',6'-trihydroxy-3'-(3-methyl-2-butenyl)acetophenone in the form of a yellow prism.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106871
Source datasetuspto-grants-1992_04
ORD IDord-74e2a1ebf3ec4cde92c5887a9a38f149
Source noteuspto-grants-1992_04