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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842987Generated: October 31, 2026

Trifluoroacetic acid → 2-(4-(Ethylsulfonamidomethyl)-3-fluorophenyl)propanoic acid

https://huagongshe.com/reaction/1842987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoateHCID 70816333—
CatalystManganeseHCID 23930—
SolventDimethylformamideHCID 6228—
Product2-(4-(Ethylsulfonamidomethyl)-3-fluorophenyl)propanoic acidHCID 70816569—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate (305 mg, 1.03 mmol) in DMF, manganese (113 mg, 2.06 mmol), NiBr2bipy (27 mg, 0.07 mmol), ethyl-2-chloro propionate (0.17 mL, 1.34 mmol) was added, followed by addition of TFA (0.002 mL, 0.028 mmol). The mixture was stirred for 1 day at 65° C. The reaction mixture was quenched by conc. HCl (7-drops) and then extracted with diethyl ether, dried (MgSO4) and the solvent was evaporated in vacuo. The residue was purified by CC (EtOAc/n-hexane). 2-(4-(ethyl-sulfonamidomethyl)-3-fluorophenyl)propanoic acid in pure form (65 mg, 20%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946204B2
Source datasetuspto-grants-2015_02
ORD IDord-5a0a674743504fb2a83b21ff1159eeaf
Source noteuspto-grants-2015_02