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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587252Generated: October 25, 2026

Water → 3-(Hexyloxy)-6-hydroxybenzene-1,2-dicarbonitrile

https://huagongshe.com/reaction/1587252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-BromohexaneHCID 8101—
ReactantPotassium HydroxideHCID 14797—
Reactant2,3-DicyanohydroquinoneHCID 78467—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product3-(Hexyloxy)-6-hydroxybenzene-1,2-dicarbonitrileHCID 1500668931.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

27 g (168.8 mM) of 2,3-dicyanohydroquinone and 22.2 g (337 mM) of 85%-potassium hydroxide were dissolved in a mixture solvent of 65 ml of methanol and 302 ml of dimethylformamide, followed by heating to 50° C. To the solution, 33.4 g (202.4 mM) of hexyl bromide were added dropwise in 25 minutes, followed by heating to 100° C. and stirring for 3 hours. The reaction mixture was poured into cold water and washed with ether. The water layer was acidified with 6N-hydrochloric acid to provide a pH value of 1, followed by precipitation of a crystal. The crystal was extracted with ether, and the ether layer was washed with 5%-sodium hydrogen-carbonate aqueous solution and further washed with water, followed by distilling-off of the solvent to obtain a crude product. The crude product was treated with activated carbon and recrystalized from methanol to obtain 13.1 g of 2,3-dicyano-4-hexyloxyphenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217643
Source datasetuspto-grants-1993_06
ORD IDord-1ef0cb99e25d4ae5bf721947c31adc49
Source noteuspto-grants-1993_06