HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389930Generated: October 25, 2026
Benzaldehyde → alpha-[(2,4,5-Trichlorophenyl)amino]benzeneacetonitrile
https://huagongshe.com/reaction/1389930
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 2,4,5-Trichloroaniline | HCID 12487 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Water | HCID 962 | — |
| Product | alpha-[(2,4,5-Trichlorophenyl)amino]benzeneacetonitrile | HCID 20296018 | — |
Reaction Steps
To a stirred mixture of 53 parts of benzaldehyde in 820 parts of water are added successively 78.6 parts of 2,4,5-trichlorobenzenamine, 81.8 parts of zinc chloride and 32.6 parts of potassium cyanide and the whole is stirred for 18 hours at 50° C. The reaction mixture is cooled to room temperature. The precipitated product is filtered off, triturated in 1000 parts of water, filtered off again and dissolved in 750 parts of trichloromethane. The solution is washed twice with water, dried, filtered and evaporated. The solid residue is triturated in petroleum ether, filtered off again and dried, yielding 83.1 parts of α-[(2,4,5-trichlorophenyl)amino]benzeneacetonitrile; mp. 123.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04246429 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-d1698bafec5a4e2fb43185c9e8bd4d09 |
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| Source note | uspto-grants-1981_01 |
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