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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130707Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2-(4-Methoxyphenyl)-2-methylpropanenitrile

https://huagongshe.com/reaction/130707

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIsobutyronitrileHCID 6559—
Edukt4-FluoroanisoleHCID 9987—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(4-Methoxyphenyl)-2-methylpropanenitrileHCID 21916652%

Reaktionsschritte

Add potassium bis(trimethylsilyl)amide (39.90 g, 200 mmol) to a stirred solution of 4-fluoroanisole (15.0 mL, 133 mmol), isobutyronitrile (49.0 mL, 539 mmol) and anhydrous tetrahydrofuran (150 mL). Heat the reaction to reflux under nitrogen for 72 h. Cool the reaction to room temperature, pour it into 1 N hydrochloric acid (300 mL), and extract with diethyl ether (3×100 mL). Wash the diethyl ether extracts with brine (100 mL), dry the extracts over magnesium sulfate, filter, and concentrate on a rotary evaporator to give the crude product. The crude product is purified by flash chromatography on silica gel eluting with 10% ethyl acetate/hexanes to yield 12.13 g (52%) of 2-(4-methoxy-phenyl)-2-methyl-propionitrile: TLC: Rf in 10% ethyl acetate/hexanes: 0.30; 1H NMR (CDCl3): 7.40-7.37 (m, 2H), 6.92-6.90 (m, 2H), 3.81 (s, 3H), 1.70 (s, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381719B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-ccf243a42fc24f19b931160a3d67fead
Quellennotizuspto-grants-2008_06