HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263532Generated: October 25, 2026
Hydrochloric Acid → Benzonitrile, 4,4'-thiobis-
https://huagongshe.com/reaction/263532
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4,4'-Thiodianiline | HCID 8765 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Benzene--water (1/1) | HCID 22272175 | — |
| Product | Benzonitrile, 4,4'-thiobis- | HCID 616861 | 49.4% |
Reaction Steps
Concentrated hydrochloric acid (45 ml) and ice were added to 21.7 g of 4,4'-thiodianiline to which, with ice-cooling, was subsequently added dropwise 50 ml of aqueous solution of 15.2 g sodium nitrite spending 30 minutes. Five minutes thereafter, the reaction mixture was neutralized with sodium carbonate and added dropwise to 250 ml of ice-cooled water-benzene (3:2) solution containing 22.4 g of copper (I) cyanide and 38.2 g of potassium cyanide. The reaction mixture was stirred for 2 hours while ice-cooling and then mixed with ethyl acetate to remove insoluble materials by filtration. The resulting organic layer was washed with saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate. The solvent was evaporated under a reduced pressure, and the resulting residue was subjected to silica gel chromatography and to obtain 11.7 g of bis(4-cyanophenyl) sulfide from fractions of chloroform elution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05643931 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-dd545de5ae9248b8ad8349de4a045129 |
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| Source note | uspto-grants-1997_07 |
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