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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 484242Erstellt: 23. Oktober 2026

Potassium Carbonate → 6-(2-Quinolinylmethoxy)-2-methyl-1-indanone

https://huagongshe.com/de/reaction/484242

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2-(Chloromethyl)quinolineHCID 20394—
Edukt18-Crown-6HCID 28557—
Edukt6-Hydroxy-2-methyl-2,3-dihydro-1h-inden-1-oneHCID 234338—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelHexaneHCID 8058—
Produkt6-(2-Quinolinylmethoxy)-2-methyl-1-indanoneHCID 1993572784,8%

Reaktionsschritte

A mixture of the phenol (15.16 g, 93.58 mmole) of Step D, powdered anhydrous potassium carbonate (12.93 g, 93.6 mmole), 18-crown-6 (2.47 g, 9.36 mmole) and dry acetonitrile (200 mL) is stirred at room temperature under a nitrogen for 15 minutes. 2-Chloromethylquinoline (free base, freshly prepared from 18.29 g or 102.96 mmole of the hydrochloride salt) is added in one portion and the mixture is placed in an oil bath heated at 65° C. for 11 hours (TLC, dichloromethanemethanol 9:1, UV). The solvent is removed in vacuo and the residue is partitioned between ethyl acetate and water. The organic phase is washed with brine, dried (MgSO4) and evaporated to yield an oil which solidifies upon trituration with hexane (ca. 31 g). The crude product is purified by flash chromatography (on silica Merck-60, absorbed in methylene chloride, eluted with CH2Cl2 -ethyl acetate 90:10 and 85:15) to provide 5.95 g of slightly impure material together with 24.55 g of the pure title compound (pale yellow solid, 84.8%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05229516
Quelldatensatzuspto-grants-1993_07
ORD IDord-e8a330f6c75b4e9c96984224ce086cfd
Quellennotizuspto-grants-1993_07