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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370581Generated: October 29, 2026

1,1-Bis(methylthio)-2-nitroethylene → HCID 70471124, compound

https://huagongshe.com/reaction/370581

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Bis(methylthio)-2-nitroethyleneHCID 83623—
ReactantHCID 13269217HCID 13269217—
SolventEthanolHCID 702—
ProductHCID 70471124HCID 7047112465%

Reaction Steps

According to the above procedure, by reacting 0.02 mol of 3-amino-N-[2-(5-dimethylaminomethylfuran-2-ylmethylthio)ethyl]benzamide and 0.02 mol of 1,1-bis-methylthio-2-nitroethene in 50 ml of ethanol, the 3-[N-(1-methylthio-2-nitroethenyl)amino]-N-[2-(5-dimethylaminomethylfuran-2-ylmethylthio)ethyl]benzamide is obtained in 65% yield, said compound being then dissolved in ethanol and treated with a 33% solution of methylamine in ethanol to give the 3-[N-(1-methylamino-2-nitroethenyl)amino]-N-[2-(5-dimethylaminomethylfuran-2-ylmethylthio)ethyl]benzamide as a practically pure oil. The product thus obtained is transformed into its oxalate in 95% ethanol. After crystallization from 200 ml of ethanol, the pure oxalate is obtained in 43% yield; m.p. 175°-177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04526995
Source datasetuspto-grants-1985_07
ORD IDord-81b5bbfcee274bb6aa56d34b99abaee9
Source noteuspto-grants-1985_07