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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646505Generated: November 2, 2026

Hydrochloric Acid → HCID 178439538, compound

https://huagongshe.com/reaction/1646505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Acetyl-3-hydroxy-2-propylbenzyl chlorideHCID 13781022—
ReactantHCID 178418558HCID 178418558—
CatalystTetrabutylammonium BromideHCID 74236—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 178439538HCID 17843953844.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of 0.30 g of 4-acetyl-3-hydroxy-2-propylbenzyl chloride, 0.24 g of 2,5-dimercapto-1,3,4-thiadiazole, 0.20 g of anhydrous potassium carbonate and 4 ml of methyl ethyl ketone was added a catalytic amount of tetra-n-butylammonium bromide. The mixture was stirred at 60° C. for 1 hour. After the reaction solution was rendered neutral by adding diluted hydrochloric acid thereto, it was extracted with ethyl acetate. After the extract was dried over anhydrous magnesium sulfate, the solvent was distilled off. The residue was recrystallized from isopropyl alcohol to give 0.20 g of 2-[(4-acetyl-3-hydroxy-2-propylbenzyl)thio]-5-mercapto-1,3,4-thiadiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180730
Source datasetuspto-grants-1993_01
ORD IDord-4dac4224c4c6467e9323163fad06773c
Source noteuspto-grants-1993_01