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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477874Generated: October 30, 2026

Thiophenol → HCID 19835105, compound

https://huagongshe.com/reaction/477874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantHCID 19835132HCID 19835132—
SolventAcetonitrileHCID 6342—
ProductHCID 19835105HCID 19835105—

Reaction Steps

15.5 ml (16.5 g) of thiophenol are added to a suspension of 9.35 g of 2-methylsulphinyl-4-amino-5-cyanothiazole, prepared according to example I, in 250 ml of acetonitrile, while stirring. After stirring at room temperature for another 30 minutes and leaving to stand overnight, the mixture is filtered with charcoal, after which the filtrate is evaporated. The residue is taken up in methylene chloride, after which the resulting solution is washed, successively with 2N sodium hydroxide solution and water, dried, filtered and diluted with isopropanol. After evaporating the methylene chloride the desired product crystallises in a yield of 7.62 g; m.p. 176°-18° C.; Rf (CH2Cl2) 0.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04889863
Source datasetuspto-grants-1989_12
ORD IDord-a3cb6883f659435cb211d9c0f1990818
Source noteuspto-grants-1989_12