HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215999Generated: October 27, 2026
Cyanamide → (1-{6-[Trifluoromethyl]pyridin-3-yl}ethyl)(methyl)lambda4-sulfanylidenecyanamide
https://huagongshe.com/reaction/215999
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | 5-[1-(Methylthio)ethyl]-2-trifluoromethylpyridine | HCID 24881119 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (1-{6-[Trifluoromethyl]pyridin-3-yl}ethyl)(methyl)lambda4-sulfanylidenecyanamide | HCID 44139272 | — |
Reaction Steps
solution of 110.6 g (0.475 mol, 95% assay) of 3-[1-(methylthio)ethyl]-6-(trifluoromethyl)pyridine and 25.2 g (0.6 mol) of cyanamide in 600 mL of acetonitrile was cooled to −5° C. To this solution was added 750 g (0.575 mol, Clorox™ 5.7% wt) of aqueous NaOCl dropwise over 45 min with the temperature kept below 0° C. The reaction mixture was allowed to stir at −1° C. for 30 min To the mixture was added 9.5 g (0.05 mol) of sodium metabisulfite in 25 mL of water and the two phase mixture was allowed to settle. The aqueous phase was re-extracted 2×'s with 50 mL of acetonitrile. The organics were combined and this acetonitrile/sulfilimine solution was used directly in the following oxidation. LC analysis indicated a 40:54 (area) ratio of two isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193222B1 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-dab76a547c634406aef6d3fa12e4d8c3 |
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| Source note | uspto-grants-2012_06 |
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