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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 220737Erstellt: 25. Oktober 2026

Toluene → 4-Methyl-1-(4-(trifluoromethyl)phenyl)pentan-1-one

https://huagongshe.com/reaction/220737

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktTetrahydrofuranHCID 8028—
Edukt1-BromopentaneHCID 8057—
EduktBenzonitrile, 4-(trifluoromethyl)-HCID 67995—
EduktMagnesiumHCID 5462224—
LösungsmittelWaterHCID 962—
Produkt4-Methyl-1-(4-(trifluoromethyl)phenyl)pentan-1-oneHCID 46941396—

Reaktionsschritte

Magnesium (17 g) was stirred 10 min under nitrogen then THF (400 mL) was added. 1-Bromo-4 -methylbutane (5 mL) was added and the mixture stirred 5 min until the reaction initiated (exotherm) the reminder of the bromomethylbutane (100 g, 0.672 mol) was added keeping the temp below 35° C. (water bath). The mixture was stirred 1 hr at RT and a solution of 4-trifluoromethylbenzonitrile (100 g, 0.584 mol) in toluene (1 L) containing some CuBr was added dropwise keeping the temp 25° C. The solution was stirred 1 h and quenched carefully with 15% H2SO4 (exotherm). The organic layer was decanted, washed with brine, dried over (MgSO4) and concentrated in vacuo. The oil was purified by column chromatography on silica using isohexane as eluant to give 4-methyl-1-[4-(trifluoromethyl)phenyl]pentan-1-one (126 g) which solidified on standing. 1H NMR δ (ppm)(CDCl3): 8.06 (2H, d, J 8.1 Hz), 7.73 (2H, d, J 8.1 Hz), 2.99 (2H, app. t, J 7.4 Hz), 1.68-1.60 (3H, m), 0.96 (6H, d, J 6.3 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08203004B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-2abcdfc4e3864f97a79dfbc0f8bf4cac
Quellennotizuspto-grants-2012_06