HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043716Generated: October 29, 2026
Potassium Cyanide → 2,5-Dichlorobenzyl cyanide
https://huagongshe.com/reaction/2043716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 2,5-Dichlorobenzyl bromide | HCID 3495744 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,5-Dichlorobenzyl cyanide | HCID 3531200 | 83.6% |
Reaction Steps
A mixture of 2,5-dichlorobenzyl bromide (5.4 g, 22.5 mmol) in 16 mL of ethanol and potassium cyanide (1.63 g, 25 mmol) in 4 mL of water was heated at 80° C. overnight, then cooled, and the solids were filtered and washed with ethanol to give 3.5 g of 2,5-dichlorophenylacetonitrile as a white powder melting at 89-91° C. The nitrile was suspended in 20 red, of ethanol, and 20 mL of a 25% aqueous NaOH solution was added. The mixture was heated in a CEM Explore™ microwave reactor at 140° C. for 30 minutes, then cooled, poured into ice water and acidified to pH 1 with concentrated HCl to give a precipitate. The precipitate was filtered, washed with water and dried in a vacuum oven at 90° C. for 5 h to give the title compound as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586611B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-1650e19846b54c33875d992443f0bb64 |
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| Source note | uspto-grants-2013_11 |
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