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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628509Generated: October 29, 2026

Hydrochloric Acid → HCID 82112865, compound

https://huagongshe.com/reaction/628509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant1-(4-Methoxy-3-methylphenyl)ethan-1-oneHCID 24806—
CatalystDibenzo-18-crown-6HCID 26541—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 82112865HCID 82112865—

Reaction Steps

At room temperature, to tetrahydrofuran 50 ml was added 55% sodium hydride 3.07 g and ethyl acetate 5.90 g and the resulting mixture was stirred for a half hour. Then, thereto was added 1 (4 methoxy-3-methylphenyl)-ethanone (described in Reference Preparation example 48) 5.50 g, dibenzo-18-crown-6 0.024 g and ethanol 1 ml and the resulting mixture was stirred with heating under reflux for six hours. To the reaction mixture was added water and the resulting mixture was acidified with aqueous 10% hydrochloric acid solution and was extracted with ethyl acetate. The organic layer was washed with water and was dried over anhydrous magnesium sulfate, and was then concentrated under reduced pressure. The resulting residue was subjected to a silica gel column chromatography to give 1-(4-methoxy-3-methyl-phenyl)-butane-1,3-dione 6.50 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09314023B2
Source datasetuspto-grants-2016_04
ORD IDord-749fad6529434d6d91c7a2230e0a1966
Source noteuspto-grants-2016_04