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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 482245Erstellt: 23. Oktober 2026

Benzyl Bromide → 3-Benzyloxy-6,7-dimethoxy-quinoline

https://huagongshe.com/de/reaction/482245

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktSodium hydrideHCID 24758—
Edukt2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Edukt6,7-Dimethoxyquinolin-3-olHCID 10058766—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Benzyloxy-6,7-dimethoxy-quinolineHCID 10085863—

Reaktionsschritte

To 3-hydroxy-6,7-dimethoxyquinoline (150 mg; 0.73 mmol) in 3 mL THF is added benzyl bromide (0.13 mL; 188 mg; 1.10 mmol) and NaH (59 mg; 1.46 mmol). This is stirred at room temperature for 1 hour and 25 mg of NaH added followed by 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)pyrimidinone (DMPU) (255 mg; 2.07 mmol) and stirred at room temperature for 31/2 hours. The reaction mixture is partitioned between EtOAc and distilled H2O and extracted 2× with EtOAc. The latter is washed with brine, dried (MgSO4), filtered, evaporated to dryness and chromatographed with 1% MeOH/CHCl3 to obtain 3-benzyloxy-6,7-dimethoxyquinoline m.p. 146.5°-148.5° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05795889
Quelldatensatzuspto-grants-1998_08
ORD IDord-5edbacb9a58941fc899bdf83916ca751
Quellennotizuspto-grants-1998_08