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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Bis(methylthio)-2-nitroethylene | HCID 83623 | — |
| Reactant | HCID 13269217 | HCID 13269217 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70471124 | HCID 70471124 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04526995 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-81b5bbfcee274bb6aa56d34b99abaee9 |
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| Source note | uspto-grants-1985_07 |
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