HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660052Generated: November 1, 2026
Hydrochloric Acid → 2-(2-(3-(Trifluoromethyl)phenylsulfonyl)ethylthio)nicotinic acid
https://huagongshe.com/reaction/660052
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloroethyl-[3-(trifluoromethyl)phenyl]sulphone | HCID 2736506 | — |
| Reactant | HCID 178524460 | HCID 178524460 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(2-(3-(Trifluoromethyl)phenylsulfonyl)ethylthio)nicotinic acid | HCID 2821392 | 88.4% |
Reaction Steps
683 mg (4.92 mmol) of K2CO3 were added to a suspension of 349 mg (2.25 mmol) of 2-mercaptonicotinic acid in DMF (5 ml), and the mixture was stirred for 30 min at RT. 614 mg (2.25 mmol) of 2-chloroethyl-(3-(trifluoromethyl)phenyl)sulfone were then added, and stirring was continued for a further 72 h at RT. The reaction solution was concentrated in vacuo, the residue obtained was taken up in ethyl acetate, and water was added. The pH was adjusted to 3 with 2 M hydrochloric acid, and the phases were separated. The aqueous phase was extracted with ethyl acetate. The combined organic phases were dried over MgSO4, filtered and concentrated in vacuo. 778 mg (1.99 mmol, 88%) of 2-(2-(3-(trifluoromethyl)phenylsulfonyl)ethylthio)nicotinic acid were obtained as residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084470B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-d01fe1f38a9343b5b7ab2a489df79fba |
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| Source note | uspto-grants-2011_12 |
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