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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211232Generated: October 30, 2026

4-Cyanophenol → 4-[(2-Methylbut-3-yn-2-yl)oxy]benzonitrile

https://huagongshe.com/reaction/2211232

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanophenolHCID 13019—
ReactantAcetic acid, trifluoro-, 1,1-dimethyl-2-propynyl esterHCID 11830027—
SolventWaterHCID 962—
Product4-[(2-Methylbut-3-yn-2-yl)oxy]benzonitrileHCID 2779072—

Reaction Steps

The 1,1-dimethyl-2-propynyl trifluoroacetate solution, maintained at 0° C., was added to the 4-cyanophenol solution over a 35 minute period while keeping the temperature at ~0° C. The resulting mixture was stirred at ~0° C. (ice bath). After stirring for 90 minutes, water (10 mL) was added and the resulting mixture was concentrated at reduced pressure. The residue was partitioned between water (50 mL) and toluene (300 mL). The organic fraction was washed with 1N HCl (3×50 mL), 1N NaOH (2×50 mL), 1N NaHCO3, and brine. After drying (magnesium sulfate), the solvent was removed at reduced pressure to give crude title compound as a yellow oil. Distillation of the crude material (bulb to bulb) afforded the title compound as a colorless, low melting solid (8.93 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05463059
Source datasetuspto-grants-1995_10
ORD IDord-627fbe6701bd499a8d4d5943c117a551
Source noteuspto-grants-1995_10