HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347632Generated: October 25, 2026
Hydrochloric Acid → 4-Bromo-2,6-dimethylbenzonitrile
https://huagongshe.com/reaction/347632
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Bromo-2,6-xylidine | HCID 90549 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromo-2,6-dimethylbenzonitrile | HCID 10910795 | — |
Reaction Steps
4-Bromo-2,6dimethylaniline (4.49 g, 22.4 mmol) was taken up in water (25 ml) and concentrated hydrochloric acid (8.0 ml) was added. The mixture was sonicated to form a fine suspension and then cooled to 0° C. A solution of sodium nitrite (1.67 g, 24.2 mmol) in water (5 ml) was then added dropwise so as to maintain the temperature of the reaction between 0–5° C. The mixture was stirred at 0–5° C. for ½ h and then neutralised by addition of solid sodium carbonate. The resulting solution was then added portionwise to a solution of copper cyanide (2.42 g, 27.0 mmol) and potassium cyanide (3.65 g, 56.1 mmol) in water (25 ml) at 70° C. The mixture was stirred at 70° C. for ½ h, allowed to cool and then extracted with toluene (2 times). The combined extracts were washed with water and brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography on silica (eluant EtOAc:pet. ether 5:95) to give an orange solid; yield 3.2 g (68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176195B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-f68d93a22edb4c43998a912d20a81b04 |
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| Source note | uspto-grants-2007_02 |
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