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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817871Generated: October 30, 2026

Trifluoroacetic acid → 5-(Ethylsulfonyl)pyridin-2-amine

https://huagongshe.com/reaction/1817871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium SulfiteHCID 24437—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-(Ethylthio)pyridin-2-amineHCID 11521117—
SolventDichloromethaneHCID 6344—
Product5-(Ethylsulfonyl)pyridin-2-amineHCID 2841170597%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-(ethylthio)pyridin-2-amine (Step A, 1.23 g, 7.96 mmol) in dichloromethane (30 mL) were added trifluoroacetic acid (1.2 mL, 15.9 mmol) and m-chloroperbenzoic acid (4.3 g, 17.5 mmol) at 0° C. The mixture was stirred at 0° C. for 2 h. Aqueous sodium sulfite (20 mL) was added. The mixture was extracted with dichloromethane (30 mL×3) and washed with aqueous sodium hydrogencarbonate (15 mL×2). The organic extracts were dried over sodium sulfate and concentrated to afford the title compound (1.43 g, 97%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598393B2
Source datasetuspto-grants-2009_10
ORD IDord-4db708d1222b4f22bdc08c63d1e81ffa
Source noteuspto-grants-2009_10