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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073779Generated: October 26, 2026

Thiophenol → 2-Amino-5-phenylthio-1,3,4-thiadiazole

https://huagongshe.com/reaction/1073779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Amino-5-bromo-1,3,4-thiadiazoleHCID 3650883—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-Amino-5-phenylthio-1,3,4-thiadiazoleHCID 1469506879.4%

Reaction Conditions

Temperature82 °C

Reaction Steps

In a mixture of 20 ml of water and 30 ml of ethanol, 7.3 g of thiophenol and 4.5 g of potassium hydroxide were added. To this solution, 11.7 g of 2-amino-5-bromo-1,3,4-thiadiazole was added, and the mixture was heated to 82° C. and stirred for 2 hours. After cooling, water was added and the mixture was filtered. The residue was washed with water and n-hexane respectively, dried under reduced pressure, and thus 10.8 g of 2-amino-5-phenylthio-1,3,4-thiadiazole was obtained. m.p. 202°~203° C. Yield 77%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971971
Source datasetuspto-grants-1990_11
ORD IDord-34899434824746c1807ad518bddb1c91
Source noteuspto-grants-1990_11