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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357320Generated: October 30, 2026

Potassium Carbonate → 4-(4-(2-Amino-2-methylpropyl)phenoxy)benzonitrile

https://huagongshe.com/reaction/357320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorobenzonitrileHCID 14517—
ReactantDimethylacetamideHCID 31374—
Reactant4-(2-Amino-2-methylpropyl)phenol acetic acidHCID 21923250—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-(4-(2-Amino-2-methylpropyl)phenoxy)benzonitrileHCID 22147771—

Reaction Conditions

Temperature134 °C

Reaction Steps

A mixture of 4-(2-amino-2-methylpropyl)phenol acetic acid salt (45.06 g, 200 mmol), powdered K2CO3 (69.1 g, 500 mmol), and DMAC (550 mL) was heated to 75°-100° C. Toluene (166 mL) was added, and the mixture was slowly heated to reflux at 134° C. The reflux temperature was raised by distillation of toluene and water into a water trap until the temperature reached 141° C. The mixture was then allowed to cool to below 100° C. at which point 4-fluorobenzonitrile (24.46 g, 202 mmol) was added along with 50 mL of toluene. The mixture was again heated to reflux at 140° C. with water being collected in a toluene-filled water trap for 4 h. The mixture was allowed to cool to room temperature, and the solids were filtered and rinsed with toluene. The filtrate was concentrated on a rotary evaporator to 77 g of syrup which was dissolved in EtOAc (400 mL). This solution was extracted with water (400 mL), and the aqueous layer was back-extracted with EtOAc (100 mL). The combined organic layers were washed with water (3×400 mL) and concentrated in vacuo to 53.4 g (100%) of oil which was >98% pure by HPLC analysis: 1H NMR (300 MHz, DMSO-d6) NMR was consistent with the desired product;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840738
Source datasetuspto-grants-1998_11
ORD IDord-7d4148fbc969499790eceb2a09b73397
Source noteuspto-grants-1998_11