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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098899Generated: October 25, 2026

1,1,1-Trifluoro-N-phenylmethanesulfonamide → Ethyl 3-chloro-4-(trifluoromethylsulfonyloxy)benzoate

https://huagongshe.com/reaction/2098899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-Trifluoro-N-phenylmethanesulfonamideHCID 68012—
ReactantEthyl 3-chloro-4-hydroxybenzoateHCID 12652105—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-chloro-4-(trifluoromethylsulfonyloxy)benzoateHCID 57467588—

Reaction Steps

A mixture of ethyl 3-chloro-4-hydroxybenzoate (available from Aldrich) (5.00 g, 25.0 mmol), N-phenyltriflamide (9.30 g, 26.0 mmol) and TEA (4.2 mL, 30.0 mmol) in DCM (40 mL) with a catalytic amount of DMAP, was stirred at ambient temperature overnight. DCM (150 mL) was added, and the reaction mixture was washed with brine (30×3 mL), dried over MgSO4, and the solvent was removed under reduced pressure. The product T1.5 was used in the next step without further purification. MS ESI (pos.) m/e: 335.0 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450522B2
Source datasetuspto-grants-2013_05
ORD IDord-8e2f460777f14bc0ad88eb2904c33301
Source noteuspto-grants-2013_05