HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925480Generated: October 28, 2026
Trifluoroacetic anhydride → 5-[1-(Methylsulfonimidoyl)ethyl]-2-(trifluoromethyl)pyridine
https://huagongshe.com/reaction/1925480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 86633708 | HCID 86633708 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-[1-(Methylsulfonimidoyl)ethyl]-2-(trifluoromethyl)pyridine | HCID 59218628 | 77.1% |
Reaction Steps
To a stirred solution of methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-λ4-sulfanylidenecyanamide (5 g, 18 mmol) in CH2Cl2 (300 mL) at 0° C. was added trifluoroacetic anhydride (7.5 mL, 54 mmol). The mixture was allowed to react at 25° C. until the starting material was fully consumed. The reaction mixture was concentrated in vacuo, dissolved in methanol (125 mL) and treated with potassium carbonate (12.5 g, 90 mmol). The mixture was allowed to stir at 25° C. until the starting material was consumed. The crude reaction mixture was filtered, concentrated and purified by chromatography (acetone-hexanes) to furnish 5-[1-(methylsulfonimidoyl)ethyl]-2-(trifluoromethyl)pyridine as a white solid (3.5 g, 77%): ESIMS m/z 253 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178685B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-096c41df65814f419a63e0e413e47d4e |
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| Source note | uspto-grants-2012_05 |
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