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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloroethyl-[3-(trifluoromethyl)phenyl]sulphoneHCID 2736506—
ReactantHCID 178524460HCID 178524460—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(2-(3-(Trifluoromethyl)phenylsulfonyl)ethylthio)nicotinic acidHCID 282139288.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084470B2
Source datasetuspto-grants-2011_12
ORD IDord-d01fe1f38a9343b5b7ab2a489df79fba
Source noteuspto-grants-2011_12