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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432966Generated: October 31, 2026

Ethyl Acetate → N-(3-amino-4-fluorophenyl)-1-chloromethanesulfonamide

https://huagongshe.com/reaction/432966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactantchloro-N-(4-fluoro-3-nitrophenyl)methanesulfonamideHCID 18760842—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
ProductN-(3-amino-4-fluorophenyl)-1-chloromethanesulfonamideHCID 1876084594%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 12.5 g of iron powder (223 mmol) and 16 mL of an aqueous solution of acetic acid (8%) was heated to 80° C., and a solution of 6 g of I -chloro-N-(4-fluoro-3-nitrophenyl)methanesulfonamide (22.3 mmol) in 20 mL of glacial acetic acid and 22 mL ethyl acetate was added dropwise to the mixture. After heating for 1.5 h the reaction mixture was filtered through a pad of Celite® and washed with 200 mL of ethyl acetate and water (twice with 25 mL). The organic phase was separated, dried (MgSO4), filtered and concentrated under reduced pressure to yield 5 g (94%) of the title compound as a solid melting at 128-129° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664400B2
Source datasetuspto-grants-2003_12
ORD IDord-bef168359c1344ba9cf349bd425414a3
Source noteuspto-grants-2003_12