HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847540Generated: October 25, 2026
Nitrite → 3,4-Bistrifluoromethylbenzonitrile
https://huagongshe.com/reaction/847540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrite | HCID 946 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3,4-Bis(trifluoromethyl)aniline | HCID 1548579 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Catalyst | Nickel Sulfate | HCID 24586 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,4-Bistrifluoromethylbenzonitrile | HCID 14793271 | 63% |
Reaction Steps
229 g (1 mole) of 3,4-bistrifluoromethyl-aniline were diazotized in a solution of 350 g of concentrated sulphuric acid in 1.25 1 of water using 70 g of sodium nitrite in 140 ml of water. After the diazonium salt solution had become nitrite-free, it was added dropwise to a solution of 550 ml of water, 210 g of sodium cyanide, 10 g of copper (I) cyanide, 500 g of sodium hydrogen carbonate and 9 g of nickel sulphate ×7 H2O heated to 100° C. The product was isolated from the reaction mixture by steam distillation and subsequently distilled again. 152 g of product having a boiling point at 14 mbar of 85° C. and a melting point of 71° to 72° C. were obtained. This corresponds to a yield of 63% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05142092 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-0c4b417b96ef4ab5af5fca5c67cd6ce8 |
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| Source note | uspto-grants-1992_08 |
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