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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228164Generated: October 25, 2026

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

https://huagongshe.com/reaction/228164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsobutyronitrileHCID 6559—
Reactant4-FluoroanisoleHCID 9987—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Methoxyphenyl)-2-methylpropanenitrileHCID 21916652%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560463B2
Source datasetuspto-grants-2009_07
ORD IDord-f3dcd6e3ee9947f6902923fb0c4cec45
Source noteuspto-grants-2009_07