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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881680Generated: October 27, 2026

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

https://huagongshe.com/reaction/1881680

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

4-(Methylamino)butanoic acid hydrochloride (10, 15.1 g, 98.1 mmol) was added to a solution of KOH (16.5 g, 294 mmol) in H2O (75 ml) and the reaction mixture was cooled in an ice bath. A solution of 3-(trifluoromethyl)benzenesulfonyl chloride (9, 12.0 g, 49.1 mmol) in THF (75 ml) was added dropwise to the reaction mixture and the mixture was stirred at room temperature overnight. Aqueous 6 M HCl (75 ml) was added, while cooling with an ice bath, and the addition of CH2Cl2 then followed. The organic phase was separated, washed with sat. NaCl solution, dried over Na2SO4 and concentrated and the residue was co-evaporated with a minimal amount of diethyl ether. Recrystallization of the residue from ethyl acetate/heptane gave AC-13 (11.32 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318769B2
Source datasetuspto-grants-2012_11
ORD IDord-9dd01cbddaad4526b78311ea808ed479
Source noteuspto-grants-2012_11