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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193049Generated: October 25, 2026

Hydrochloric Acid → 1-(1,3-Dioxolan-2-ylmethyl)quinoxalin-2(1h)-one

https://huagongshe.com/reaction/2193049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2(1H)-QuinoxalinoneHCID 14526—
ReactantSodium hydrideHCID 24758—
Reactant1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(1,3-Dioxolan-2-ylmethyl)quinoxalin-2(1h)-oneHCID 59398152—

Reaction Conditions

Temperature40 °C

Reaction Steps

To 20 mL of an N,N-dimethylformamide suspension containing 2.0 g of quinoxalin-2(1H)-one, 0.82 g of 60% sodium hydride was dividedly added at room temperature, and the mixture was stirred at 40° C. for 15 minutes. Thereto was added 2.1 mL of 2-bromomethyl-1,3-dioxolane, and the mixture was stirred at 60° C. for 30 minutes, and stirred at 110 to 120° C. for 1 hour. Thereto was added 2.1 mL of 2-bromomethyl-1,3-dioxolane, and the mixture was stirred at 110 to 120° C. for 5 hours. The reaction mixture was cooled to room temperature, ethyl acetate and water were added, and the resultant solution was adjusted to pH 2.0 with 6 mol/L hydrochloric acid. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed sequentially with water and an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; hexane:ethyl acetate 1:2] to obtain 1.5 g of a light brown oily substance, 1-(1,3-dioxolan-2-ylmethyl)quinoxalin-2(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329694B2
Source datasetuspto-grants-2012_12
ORD IDord-454b412c531d4d1bb8c2febe5dfa1a7a
Source noteuspto-grants-2012_12