Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2094822Generated: October 31, 2026

Trifluoroacetic anhydride → 5-[1-(Methylsulfonimidoyl)ethyl]-2-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/2094822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86633708HCID 86633708—
SolventDichloromethaneHCID 6344—
Product5-[1-(Methylsulfonimidoyl)ethyl]-2-(trifluoromethyl)pyridineHCID 5921862877.1%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445689B2
Source datasetuspto-grants-2013_05
ORD IDord-9e135b75f11b4af4ab2fbe9ced735b7c
Source noteuspto-grants-2013_05