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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268793Generated: October 31, 2026

Acetic Anhydride → N-(3-fluoro-2-methylphenyl)acetamide

https://huagongshe.com/reaction/2268793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3-Fluoro-2-methylanilineHCID 285553—
ProductN-(3-fluoro-2-methylphenyl)acetamideHCID 1489284—

Reaction Steps

3-Fluoro-2-methylaniline was acetylated with acetic acid anhydride to give 3-fluoro-2-methyl-N-acetylaniline. Displacing fluorine of the 3-fluoro-2-methyl-N-acetylaniline with methylamine followed by nitration, deacetylation and reduction of the nitro group with palladium or charcoal gave 1,2-diamino-3-methyl-4-methylaminobenzene. Condensation of 4,4′-dibromobenzil with the 1,2-diamino-3-methyl-4-methylaminobenzene in refluxing methanol gave 2,3-bis(4-bromophenyl)-5-methyl-6-methylaminoquinoxaline which upon acetylation with acetic acid anhydride, nitration, reduction with palladium on charcoal and cyclization gave the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329375B1
Source datasetuspto-grants-2001_12
ORD IDord-5e2febbf11b94a7693a8a33d2d5628f1
Source noteuspto-grants-2001_12