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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091102Generated: October 30, 2026

2-Acetylhydroquinone → HCID 66777813, compound

https://huagongshe.com/reaction/2091102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AcetylhydroquinoneHCID 10279—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromoethyl methyl etherHCID 80972—
SolventAcetonitrileHCID 6342—
ProductHCID 66777813HCID 6677781350%

Reaction Steps

To a solution (250 mL) of 1-(2,5-dihydroxyphenyl)ethanone (11.0 g) in acetonitrile were added 2-methoxyethylbromide (19.6 mL) and potassium carbonate (12.0 g) at room temperature, and the mixture was heated under reflux for 15 hr. The reaction mixture was allowed to cool to room temperature and filtered through celite, and the filtrate was concentrated under reduced pressure. Saturated aqueous ammonium chloride solution was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:10, volume ratio) to give the title object compound (7.6 g, 50%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-649954b39a044b45b744189d910d7eaf
Source noteuspto-grants-2013_05