HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328957Generated: October 31, 2026
Potassium thiocyanate → HCID 21440137, compound
https://huagongshe.com/reaction/328957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | HCID 21440168 | HCID 21440168 | — |
| Catalyst | HCID 178514151 | HCID 178514151 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21440137 | HCID 21440137 | — |
Reaction Steps
To a mixture of potassium thiocyanate (42 g), copper thiocyanate (4s g) and water (400 ml), 2-benzoyl-5-carboxy3-nitrobenzenediazonium tetrafluoroborate (prepared as described in Example 17, step A; 28 g) is added in portions while stirring at 45°-50° C. After the addition is completed, the mixture is stirred at about 50° C. for a further 4 hours and thereafter at room temperature for about 20 hours. The resulting precipitate is collected by filtration, washed with water and dried. The dried solids are then extracted with boiling ethanol (three portions of 250 ml, 100 ml, and 100 ml, respectively) and filtered hot. The combined filtrates are evaporated in vacuo and the residue is crystallized by trituration with 50% aqueous ethanol (100 ml). The material is collected by filtration, washed with cold 50% ethanol and dried. After recrystallization from aqueous ethanol, 4-benzoyl-5-nitro-3-thiocyanobenzoic acid is obtained with a melting point of 183.5°-184.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04018794 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-8d21980089be47379960e7026299acf7 |
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| Source note | uspto-grants-1977_04 |
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