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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211225Generated: October 31, 2026

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

https://huagongshe.com/reaction/2211225

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanophenolHCID 13019—
Reactant1-Butyne, 3-chloro-3-methyl-HCID 70679—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventAcetonitrileHCID 6342—
Product4-[(2-Methylbut-3-yn-2-yl)oxy]benzonitrileHCID 2779072100.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-cyanophenol (655 g, 5.50 mol) in acetonitrile (10 L) at 0° C. under nitrogen was added cuprous chloride (495 mg, 5 mmol, 0.001 eq., 0.1 mol %). DBU (970 mL, 6.51 mol) was added slowly while maintaining the temperature at <5° C. 3-Chloro-3-methyl-1-butyne (570 mL, 5 mole) was added. After stirring for 4 hours at 0° C., the mixture was concentrated at reduced pressure and the residue was partitioned between ethyl acetate (5 L) and 1N HCl (2 L). The organic fraction was washed with 1N NaOH (2×1 L), water (1 L), and brine (1 L). After drying (magnesium sulfate), the solvent was removed at reduced pressure to afford the title compound as a yellow oil (930 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05463059
Source datasetuspto-grants-1995_10
ORD IDord-31355b9ef8a04ec48929db72cdb40389
Source noteuspto-grants-1995_10