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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604252Generated: October 29, 2026

Salicylic Acid → HCID 135510740, compound

https://huagongshe.com/reaction/604252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylic AcidHCID 338—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 57588558HCID 57588558—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductHCID 135510740HCID 13551074085%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910568B2
Source datasetuspto-grants-2011_03
ORD IDord-224ec0348b8b414d961fce0ce7208bbb
Source noteuspto-grants-2011_03