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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428770Generated: November 1, 2026

Trifluoroacetic acid → Ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate

https://huagongshe.com/reaction/1428770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl 2-chloropropionateHCID 10807—
ReactantN-(4-bromo-2-fluorobenzyl)ethanesulfonamideHCID 70816043—
CatalystManganeseHCID 23930—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoateHCID 70816333—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of N-(4-bromo-2-fluorobenzyl)ethanesulfonamide (305 mg, 1.03 mmol) in dimethylformamide, Manganese (113 mg, 2.06 mmol), (2,2′-Bipyridine)nickel(II)-dibromide (27 mg, 0.07 mmol), ethyl 2-chloropropanoate (0.17 mL, 1.34 mmol) was added. It was followed by addition of trifluoroacetic acid (0.002 mL, 0.028 mmol). The mixture was stirred for 24 h at 65° C. The reaction mixture was quenched by concentrated HCl (7 drops). Then it was extracted with diethyl ether, dried over magnesium sulfate, the solvent was evaporated in vacuo. It was purified by column chromatography to obtain ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate in pure form (65 mg, 20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-7edd26114cc04e33bfd956ab2d6f7af1
Source noteuspto-grants-2015_01