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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435172Generated: October 29, 2026

Thiophenol → HCID 178518535, compound

https://huagongshe.com/reaction/435172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantSodiumHCID 5360545—
ReactantHCID 178517818HCID 178517818—
SolventMethanolHCID 887—
ProductHCID 178518535HCID 17851853570.5%

Reaction Steps

To a solution of 2.3 g (0.10 m) of sodium metal dissolved in 125 ml of methanol was added a solution of 5.51 g (0.05 m) of thiophenol in 25 ml of methanol. To this mixture was added 9.8 g (0.05 m) of 1-(2-pyridinyl)-5-chloro-1H-1,2,4-triazol-3-ol and the mixture stirred for three hours at toom temperature. The methanol was removed by evaporation under vacuum and the residue which remained was taken up in water and the water insoluble solids were removed by filtration. The aqueous layer was acidified with concentrated hydrochloric acid. The white solid which precipitated was recovered by filtration and dried under vacuum to yield 9.5 g (~70 percent of theoretical) of the desired 1-(2-pyridinyl)-5-(phenylthio)-1H-1,2,4-triazol-3-ol product. The product melted at 235°-237° C. and upon analysis was found to have carbon, hydrogen and nitrogen contents of 55.87, 3.79 and 19.90 percent, respectively, as compared with the theoretical contents of 55.91, 3.93 and 20.06 percent, respectively, calculated for the above named compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04400516
Source datasetuspto-grants-1983_08
ORD IDord-730d3cf516f3425e85b2cf0d41f38d04
Source noteuspto-grants-1983_08