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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1948728Erstellt: 25. Oktober 2026

8-Methyl-2-phenylquinoline-3-carboxaldehyde → HCID 67197756, Verbindung

https://huagongshe.com/reaction/1948728

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt8-Methyl-2-phenylquinoline-3-carboxaldehydeHCID 833680—
EduktHCID 178418348HCID 178418348—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 67197756HCID 6719775665%

Reaktionsschritte

To a solution of 8-methyl-2-phenylquinoline-3-carboxaldehyde (211 mg, 0.85 mmol) in THF (6 mL) cooled to −78° C. was added methyllithium (1.6N solution in ether, 0.6 mL, 0.93 mmol). After 1 h a further portion of methyllithium (0.2 mL, 0.32 mmol) was added. The reaction was allowed to warm to r.t. before being quenched with water (10 mL). The THF was removed in vacuo and the residue partitioned between DCM (100 mL) and water (30 mL). The organic layer was separated, dried (MgSO4) and concentrated in vacuo. Purification by column chromatography (SiO2, 5-25% EtOAc in heptane) gave the title compound as a white solid (145 mg, 65%). δH (CDCl3) 8.42 (s, 1H), 7.70 (d, J 12 Hz, 1H), 7.60-7.63 (m, 2H), 7.42-7.55 (m, 5H), 5.23-5.31 (m, 1H), 2.80 (s, 3H), 1.87 (d, J 3.6 Hz, 1H), 1.47 (d, J 6.4 Hz, 3H). LCMS (ES+) 264.16 (M+H)+, RT 4.03 minutes (Method 4).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08399483B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-28319f5592994a859bd5d9a8b0630a8e
Quellennotizuspto-grants-2013_03