Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 226938Erstellt: 24. Oktober 2026

m-Xylyl bromide → 3-(3,4-Dimethyl-benzoyl)-1-(3-methyl-benzyl)-2,3-dihydro-1H-quinolin-4-one

https://huagongshe.com/de/reaction/226938

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-Xylyl bromideHCID 12099—
EduktSodium hydrideHCID 24758—
Edukt3-(3,4-Dimethyl-benzoyl)-1H-quinolin-4-oneHCID 57754515—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(3,4-Dimethyl-benzoyl)-1-(3-methyl-benzyl)-2,3-dihydro-1H-quinolin-4-oneHCID 67072135—

Reaktionsschritte

Compound 4m was prepared following the procedure outlined in Step 3 of Example 1 using 16 mg (0.4 mmol) of sodium hydride (60%), 86 mg (0.31 mmol) of 3-(3,4-dimethyl-benzoyl)-2,3-dihydro-1H-quinolin-4-one 3a, 3 mL of anhydrous dimethylformamide, and 74.0 mg (0.40 mmol) of 3-methylbenzylbromide. The crude product 4m was purified by flash chromatograph to yield 55 mg of colorless solid: LC-MSD, m/z for C26H23NO2, [M+H]+: 382.5, [M+H]+: 383.5; Reverse phase HPLC (gradient acetonitrile 0.1% TFA 20-95% in 4 min) retention time=2.628 min; 1H NMR (400 MHz, CDCl3/HCl): δ 2.3-2.4 (t, 9H), 5.4 (s, 2H), 7.0 (d, 2H), 7.12 (d, 1H), 7.18 (d, 1H), 7.25 (d, 1H), 7.4 (t, 2H), 7.58 (m, 2H), 7.65 (s, 1H), 8.26 (s, 1H), 7.48 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07557213B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-d1cbefff430f4df5b2e42ab307128bfc
Quellennotizuspto-grants-2009_07