Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426678Generated: October 31, 2026

Ethanol → HCID 178485018, compound

https://huagongshe.com/reaction/426678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantCysteamine HydrochlorideHCID 9082—
ReactantSodium HydroxideHCID 14798—
ReactantN-cyano-N,S-dimethyl-isothioureaHCID 21660514—
SolventWaterHCID 962—
ProductHCID 178485018HCID 178485018—

Reaction Steps

A solution of cysteamine hydrochloride (5.68 g) in water (20 ml) was added to a suspension of N-cyano-N,S-dimethylisothiourea (6.46 g) in ethanol (100 ml). A solution of sodium hydroxide (4.0 g) in water (20 ml) was added to the mixture and the suspension was heated under reflux for one hour. The resulting clear solution was concentrated to remove ethanol, a little more water was added and the alkaline aqueous solution was extracted with ethyl acetate. The aqueous solution was adjusted to pH4 with hydrochloric acid and extracted with ethyl acetate. This latter organic extract was dried and evaporated to give N-cyano-N'-methyl-N"-(2-mercaptoethyl)guanidine (6.12 g) as a colourless oil. In order to characterise this product a solution of 2,4-dinitrochlorobenzene (7.7 g) in 95% ethanol (50 ml) was added to a solution of N-cyano-N'-methyl-N"-(2-mercaptoethyl)guanidine (6.0 g) in 95% ethanol. The mixture was refluxed for one hour and cooled. The resulting crystalline solid (7.73 g) was collected and was triturated with a large volume of ether and was recrystallised from acetonitrile to afford N-cyano-N'-methyl-N"-[S-(2,4-dinitrophenyl)-2-mercaptoethyl]guanidine, m.p. 210°-211° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04171325
Source datasetuspto-grants-1979_10
ORD IDord-4aad1456056f477283ccd86eb813d262
Source noteuspto-grants-1979_10