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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264749Generated: October 26, 2026

Acetic Anhydride → 5-Bromo-2-methoxybenzonitrile

https://huagongshe.com/reaction/264749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactant5-Bromo-2-methoxybenzaldehydeHCID 90684—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
Product5-Bromo-2-methoxybenzonitrileHCID 4418560—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-Bromo-o-anisaldehyde (6.45 g), hydroxylamine hydrochloride (2.2 g), sodium acetate (4.1 g) and acetic acid (20 mL) was heated at 100 ° C. with stirring for 1 h. Acetic anhydride was added (20 mL) and the mixture was refluxed for 8 h. The reaction mixture was poured onto ice water and the mixture was made basic by the careful addition of 50% sodium hydroxide. The product was extracted with ether, the ether extracts were dried over magnesium sulfate and the sovent was removed in vacuo. The residue was crystallized from ether/hexane to afford 5-Bromo-2-methoxy-benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646280
Source datasetuspto-grants-1997_07
ORD IDord-b6043656dfe24c09833bc4f307bc72ed
Source noteuspto-grants-1997_07