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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 552844Erstellt: 24. Oktober 2026

Hydrochloric Acid → Benzonitrile, 4-(2-methylpropyl)-3-(trifluoromethyl)-

https://huagongshe.com/de/reaction/552844

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktN-methyl-2-pyrrolidoneHCID 13387—
Edukt4-Chloro-3-(trifluoromethyl)benzonitrileHCID 2736474—
EduktHCID 178418816HCID 178418816—
KatalysatorFerric cationHCID 29936—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzonitrile, 4-(2-methylpropyl)-3-(trifluoromethyl)-HCID 59214268—

Reaktionsschritte

To a solution of 4-chloro-3-(trifluoromethyl)benzonitrile (1 g) and iron(3+) tris[(2Z)-4-oxopent-2-ene-2-oleate] (86 mg), and 1-methylpyrrolidin-2-one (2.8 ml) in THF (30 ml) was added a solution of 2M bromo(isobutyl)magnesium in diethyl ether (2.9 ml) under ice-cooling. The solution was stirred at room temperature for 30 minutes, and diluted with diethyl ether (30 ml), and then 1M HCl was carefully added thereto to complete the reaction. The reaction solution was extracted with EtOAc (100 ml), and the organic layer was dried over anhydrous MgSO4, and then filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:EtOAc=100:0 to 95:5) to obtain 4-isobutyl-3-(trifluoromethyl)benzonitrile (320 mg) as a pale yellow liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07951825B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-b4c96d15c074444f8954764aa258d494
Quellennotizuspto-grants-2011_05