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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049108Generated: November 2, 2026

Thiophenol → HCID 15593669, compound

https://huagongshe.com/reaction/2049108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
Reactant3,5-Dichloro-4H-1,2,6-thiadiazin-4-oneHCID 354026—
SolventTrimethylamineHCID 1146—
SolventDiethyl EtherHCID 3283—
ProductHCID 15593669HCID 15593669—

Reaction Steps

In one portion 2.5 g of trimethylamine was added to a solution of 4.6 g of 3,5-dichloro-4H-1,2,6-thiadiazin-4-one in 75 ml of ethyl ether in a 250 ml flask. A solution of 2.8 g of thiophenol in 25 ml of ethyl ether was then added dropwise to the flask during a 15 minute period. The reaction was allowed to stir for 3 hrs. after which it was filtered. The filter cake was washed with ether, and the filter cake was discarded. Successively, the ether solution was washed twice with 50 ml of water and once with 50 ml of saturated sodium chloride solution. The ether solution was then dried over anhydrous sodium sulfate. The ether was evaporated, leaving a solid residue which was recrystallized from 75 ml of cyclohexane. The yellow-orange 3-chloro-5-phenylthio-4H-1,2,6-thiadiazin-4-one weighed 3.6 g, mp 99.5°-101.5° C. (Lit. mp 102.5°-103.5° C., J. Geevers and W. P. Trompen, supra.) The ir spectrum was consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04196284
Source datasetuspto-grants-1980_04
ORD IDord-4dbdee6882f9403aad6f4d72e48e967f
Source noteuspto-grants-1980_04