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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 339056Erstellt: 25. Oktober 2026

Hydrochloric Acid → 8-(1,3-Dimethoxypropan-2-yloxy)-2-methylquinoline

https://huagongshe.com/reaction/339056

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriphenylphosphineHCID 11776—
Edukt1,3-Dimethoxy-2-propanolHCID 12190—
Edukt2-Methyl-8-hydroxyquinolineHCID 13224—
EduktDiisopropyl azodicarboxylateHCID 5363146—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt8-(1,3-Dimethoxypropan-2-yloxy)-2-methylquinolineHCID 7098413789,15%

Reaktionsschritte

To a solution of 2-methylquinolin-8-ol (4.10 g, 25.76 mmol), PPh3 (16.89 g, 64.39 mmol) and 1,3-dimethoxypropan-2-ol (4.02 g, 33.48 mmol) in THF (20 mL) was added DIAD (8.40 mL, 41.21 mmol) dropwise at ambient temperature. The reaction mixture was stirred at room temperature for two days. 4 N HCl (7.73 mL, 30.91 mmol in water), water (20 mL), and ethyl acetate (50 mL) were added. The aqueous layer was separated and washed with ethyl acetate. The aqueous layer was neutralized with ammonium hydroxide to about pH 9 and extracted with ethyl acetate (50 mL). The organic layer was separated, washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (1:2 hexane/ethyl acetate) to give 8-(1,3-dimethoxypropan-2-yloxy)-2-methylquinoline (6.00 g, 89.15%) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889704B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-d2d57cd034be462d8e17eb4ed307e329
Quellennotizuspto-grants-2014_11