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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193106Generated: October 25, 2026

Hydrochloric Acid → 1-(1,3-Dioxolan-2-ylmethyl)-8-methylquinolin-2(1h)-one

https://huagongshe.com/reaction/2193106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
Reactant8-methylquinolin-2(1H)-oneHCID 5325167—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(1,3-Dioxolan-2-ylmethyl)-8-methylquinolin-2(1h)-oneHCID 59398217—

Reaction Steps

To 3 mL of an N,N-dimethylformamide solution containing 0.17 g of 8-methylquinolin-2(1H)-one, 0.13 g of 60% sodium hydride was added under a nitrogen atmosphere, and the mixture was stirred at room temperature for 30 minutes. Thereto was added 0.89 g of 2-bromomethyl-1,3-dioxolane, and the mixture was stirred at 90° C. for 48 hours. The reaction mixture was cooled to room temperature, then ethyl acetate and 1 mol/L hydrochloric acid were added thereto. 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 with 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 [silica gel; Chromatorex-NH, manufactured by Fuji Silysia Chemical Ltd., eluent; hexane:ethyl acetate=8:1] to obtain 0.18 g of a pale yellow oily substance, 1-(1,3-dioxolan-2-ylmethyl)-8-methylquinolin-2(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329694B2
Source datasetuspto-grants-2012_12
ORD IDord-4d2805c60e5641d1a4a6278878d662ed
Source noteuspto-grants-2012_12