HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604252Generated: October 29, 2026
Salicylic Acid → HCID 135510740, compound
https://huagongshe.com/reaction/604252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylic Acid | HCID 338 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 57588558 | HCID 57588558 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 135510740 | HCID 135510740 | 85% |
Reaction Steps
5-(4-Amino-phenyl)-[1,2]dithiole-3-thione (3, 0.56 mmol) was dissolved in a mixture of 5 mL of concentrated HCl and 2.5 mL of water and diazotized with a solution of sodium nitrite (0.56 mmol). In the meantime salicylic acid (0.56 mmol), potassium hydroxide (1.12 mmol) and sodium carbonate are dissolved in water. The diazo suspension is added in portions to the alkaline solution of salicylic acid and the alkalinity maintained at a sufficiently high level during the whole reaction by means of addition of further quantities of potassium hydroxide solution. After 2 days the reaction mixture is heated for 30 min at 50° C. The azo compound (4) was precipitated by means of HCl and filtered off (yield 85%), to yield the compound of Formula II, 2-Hydroxy-5-[4-(5-thioxo-5H-[1,2]dithiol-3-yl)-phenylazo]-benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910568B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-224ec0348b8b414d961fce0ce7208bbb |
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| Source note | uspto-grants-2011_03 |
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