Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204924Generated: November 1, 2026

Potassium Iodide → (3,4-Diethoxyphenyl)acetonitrile

https://huagongshe.com/reaction/2204924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDimethylformamideHCID 6228—
ReactantEthyl BromideHCID 6332—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3,4-Dihydroxyphenyl)acetonitrileHCID 10909727—
SolventWaterHCID 962—
Product(3,4-Diethoxyphenyl)acetonitrileHCID 520318—

Reaction Conditions

Temperature80 °C

Reaction Steps

15.44 g (140 mmol) of bromoethane and 8.95 g (59 mmol) of 2-(3,4-Dihydroxyphenyl)-acetonitrile are dissolved in 120 mL of N,N-dimethylformamide. 19.39 g (140 mmol) of potassium carbonate and 0.97 g (6 mmol) of potassium iodide are added to the mixture and the resulting suspension is heated to 80° C. After 6 h the reaction mixture is cooled down to at least 30° C. Pour the suspension on 200 mL of icy water, stir for ca. 20 min and filter off. Digest the solid in 120 mL of water, neutralize with hydrochloric acid 25% stir for 30 min. The precipitate is filtered off, washed with water and dried under vacuum at r40° C. 4.72 g of 2-(3,4-diethoxyphenyl)-acetonitrile are obtained as a white powder (39.3% yield). This material proves chromatographically homogenous and displays spectral characteristics consistent with its assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09366906B2
Source datasetuspto-grants-2016_06
ORD IDord-afcabcef79f84dc28edad7de6e13ca2b
Source noteuspto-grants-2016_06