HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204924Generated: November 1, 2026
Potassium Iodide → (3,4-Diethoxyphenyl)acetonitrile
https://huagongshe.com/reaction/2204924
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(3,4-Dihydroxyphenyl)acetonitrile | HCID 10909727 | — |
| Solvent | Water | HCID 962 | — |
| Product | (3,4-Diethoxyphenyl)acetonitrile | HCID 520318 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09366906B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-afcabcef79f84dc28edad7de6e13ca2b |
|---|
| Source note | uspto-grants-2016_06 |
|---|