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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 5-(Ethylthio)pyridin-2-amine | HCID 11521117 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(Ethylsulfonyl)pyridin-2-amine | HCID 28411705 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598393B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-4db708d1222b4f22bdc08c63d1e81ffa |
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| Source note | uspto-grants-2009_10 |
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