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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645241Generated: October 30, 2026

Hydrochloric Acid → 4-[Methyl-[[3-(trifluoromethyl)phenyl]sulfonyl]-amino]-butyric acid

https://huagongshe.com/reaction/1645241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
Reactant4-(Methylamino)butyric acid hydrochlorideHCID 12626654—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-[Methyl-[[3-(trifluoromethyl)phenyl]sulfonyl]-amino]-butyric acidHCID 43236455—

Reaction Steps

To a solution of KOH (16.5 g, 294 mmol) in H2O (75 ml) was added 4-(methylamino)butyric acid hydrochloride (10, 15.1 g, 98.1 mmol) and the reaction mixture was cooled with an icebath. A solution of 3-(trifluoromethyl)benzene-sulfonyl chloride (9, 12.0 g, 49.1 mmol) in THF (75 ml) was dropwise added to the reaction mixture and stirring was continued at room temperature overnight. Aqueous 6 M HCl (75 ml) was added to the reaction mixture while cooling with an icebath, after which CH2Cl2 was added. The organic layer was separated, washed with brine, dried (Na2SO4), concentrated and co-evaporated with a minimal amount of Et2O. Crystallization of the residue out of EtOAc/heptane resulted in S-13 (11.32 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124624B2
Source datasetuspto-grants-2012_02
ORD IDord-5eba2e5c760843a0a2312828b3de15f1
Source noteuspto-grants-2012_02