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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421767Generated: October 27, 2026

4-(Trifluoromethyl)aniline → Ethyl 3-({[4-(trifluoromethyl)phenyl]amino}sulfonyl)benzoate

https://huagongshe.com/reaction/421767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)anilineHCID 9964—
ReactantEthyl 3-(chlorosulfonyl)benzoateHCID 19790734—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductEthyl 3-({[4-(trifluoromethyl)phenyl]amino}sulfonyl)benzoateHCID 66675205—

Reaction Steps

To ethyl 3-(chlorosulfonyl)benzoate (4.0 g, 16.08 mmol) in N,N-dimethylacetamide (20 mL) was added 4-(trifluoromethyl)aniline (10.37 g, 64.3 mmol) dropwise at room temperature. The mixture was stirred at room temperature for 2.5 hours, and then it was diluted with ethyl acetate (130 mL). The organic solution was washed with 1 N HCl (2×60 mL) and saturated NaCl (60 mL). The organic layer was concentrated, ethanol (40 mL) was added, and the mixture was concentrated to give ethyl 3-({[4-(trifluoromethyl)phenyl]amino}sulfonyl)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101614B2
Source datasetuspto-grants-2012_01
ORD IDord-3bc39a7548f34014ae8efbd9947efc87
Source noteuspto-grants-2012_01