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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862845Generated: October 31, 2026

Hydrochloric Acid → HCID 178433297, compound

https://huagongshe.com/reaction/1862845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Nitro2-methylthio-2-methylsulphinylethyleneHCID 54487094—
ReactantHCID 178433288HCID 178433288—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 178433297HCID 178433297—

Reaction Steps

A solution of 2,2,2-trifluoroethylamine (4.0 g) from the hydrochloride and potassium hydroxide in methanol (45 ml) and water (5 ml) was added slowly to a suspension of 1-nitro-2-methylsulphinyl-2-methylthio ethylene (3.6 g) in methanol (150 ml) at 0°. The mixture was stirred at room temperature for 24 hours, concentrated and dissolved in chloroform. Filtration, redissolution in a small volume of chloroform and precipitation with hexane afforded an orange crystalline solid. This was dissolved in methanol (25 ml) and a solution of 4-methyl-5-[(2-aminoethyl)thiomethyl]imidazole (2.1 g) in methanol (25 ml) was added. The resulting solution was heated under reflux for 2 hours and set aside at room temperature for 18 hours. Concentration followed by chromatographic purification on a column of silica gel with chloroform-methanol (15.1) as eluant and final crystallisation from ethanol afforded the title compound as a hemi-ethanolate (2.4 g) m.p. 161° (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04166856
Source datasetuspto-grants-1979_09
ORD IDord-0da2ab740e5549c1ad264d73f320809f
Source noteuspto-grants-1979_09