HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087131Generated: October 31, 2026
Hydrochloric Acid → 4-Chloro-2-methylbenzonitrile
https://huagongshe.com/reaction/1087131
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-2-methylbenzonitrile | HCID 142742 | — |
Reaction Steps
Toluene (30 mL) and ice was added to the above copper cyanide solution and then the reaction mixture was stirred vigorously. The above diazonium salt solution was then slowly added to the reaction mixture. After the addition was complete, the reaction mixture was stirred at 0° C. for 30 minutes. The reaction mixture was then allowed to warm to room temperature (25° C.), and then stirred for another hour. The reaction mixture was then heated to 50° C. for 2 hours without stirring. The toluene phase and precipitate were then separated from the aqueous phase. To the toluene phase was added 10 mL concentrated HCl, 40 mL hot H2O, and FeCl3.6H2O (32 g, 0.118 mol) and this reaction mixture was then stirred overnight. The reaction mixture was then added to 200 mL H2O. The organic phase was then extracted with toluene, dried and evaporated under reduced pressure to produce 4-chloro-2-methylbenzonitrile as a dark brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05034410 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-a050c3ed24de4d4bae0c2d12fb26feb1 |
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| Source note | uspto-grants-1991_07 |
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