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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2193106Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2193106

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium hydrideHCID 24758—
Edukt1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
Edukt8-methylquinolin-2(1H)-oneHCID 5325167—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(1,3-Dioxolan-2-ylmethyl)-8-methylquinolin-2(1h)-oneHCID 59398217—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08329694B2
Quelldatensatzuspto-grants-2012_12
ORD IDord-4d2805c60e5641d1a4a6278878d662ed
Quellennotizuspto-grants-2012_12