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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428716Generated: November 1, 2026

Hydrochloric Acid → Ethyl 2-(3-fluoro-4-(methylsulfonamidomethyl)phenyl)propanoate

https://huagongshe.com/reaction/1428716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl 2-chloropropionateHCID 10807—
ReactantN-(4-bromo-2-fluorobenzyl)methanesulfonamideHCID 70847718—
CatalystManganeseHCID 23930—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(3-fluoro-4-(methylsulfonamidomethyl)phenyl)propanoateHCID 7085555939.3%

Reaction Conditions

Temperature65 °C

Reaction Steps

N-(4-bromo-2-fluorobenzyl)methanesulfonamide (29 g, 102.8 mmol) and ethyl-2-chloropropionate (18.26 g, 133.6 mmol) were dissolved in dimethylformamide (155 mL) in a protective gas atmosphere at room temperature. Subsequently, manganese (11.29 g, 205.6 mmol), (2,2′-bipyridine)nickel(II) dibromide (2.69 g, 7.2 mmol) and trifluoroacetic acid (1.48 mL) were added and the mixture was stirred at 65° C. for 36 h. The reaction mixture was cooled to room temperature, hydrolysed using 1 N HCl (50 mL) and extracted with diethyl ether (4×100 mL). The combined organic layer were washed with water (40 mL) and brine solution (40 mL) and dried over magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by column chromatography (eluent: diethyl ether/n-hexane 9:1) to afford ethyl 2-(3-fluoro-4-(methylsulfonamidomethyl)phenyl)propanoate (12.27 g, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-de3d54fd924a4b7fbd8702fe252758fd
Source noteuspto-grants-2015_01