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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396767Generated: October 26, 2026

Acetic Acid → 3-Fluoro-4-(methylsulfonyl)aniline

https://huagongshe.com/reaction/396767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-Fluoro-1-(methylsulfonyl)-4-nitrobenzeneHCID 22316781—
CatalystIronHCID 23925—
SolventWaterHCID 962—
Product3-Fluoro-4-(methylsulfonyl)anilineHCID 2231660990%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 3-fluoro-4-(methylsulfonyl)nitrobenzene (8 g, 36.5 mmol), iron powder (22 g, 394 mmol), and acetic acid (0.3 mL) in water (200 mL) was heated at 95° C. for 3 hours. After cooling, insolubles were filtered off by Celite. The filtrate was extracted with ethyl acetate (200 mL×2), the combined organic layer washed with water, brine, dried over MgSO4, and concentrated in vacuo. Chromatographic purification of the residue eluting with ethyl acetate/hexane (1/1) provided the subtitle compound (6.2 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608095B2
Source datasetuspto-grants-2003_08
ORD IDord-ad14a11c528642279f3d894b74184ebc
Source noteuspto-grants-2003_08