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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841870Generated: October 25, 2026

Acetic Anhydride → 6-Bromo-8-chlorocoumarin

https://huagongshe.com/reaction/841870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant5-Bromo-3-chloro-2-hydroxybenzaldehydeHCID 2716696—
Product6-Bromo-8-chlorocoumarinHCID 22608599—

Reaction Conditions

Temperature136 °C

Reaction Steps

To a 5 L round bottom flask fitted with a mechanical stirrer and condenser was placed 3-chloro-5-bromosalicylaldehyde (554.1 g, 2.35 mol, 1 equiv.), acetic anhydride (1203 g, 11.8 mol, 5 equiv.) and triethylamine (237.4 g , 2.35 mol, 1 equiv.). The reaction solution was heated at reflux (131-141° C.) overnight. The dark brown reaction mixture was cooled to 50° C. and ice (2 L) added (ice-bath cooling) with stirring. After one hour the mixture was filtered and the filtrate combined with EtOH (1 L). To this mixture was added EtOH (300 mL) and the reaction mixture stirred for one hour. The precipitate that formed was collected by filtration and washed with water: EtOH (3×1.3 L), vacuum and dried then dried on a fluid-bed drier. The total isolated yield is 563 g or 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372719B1
Source datasetuspto-grants-2002_04
ORD IDord-a5b909c104ac4124985b508e7c508547
Source noteuspto-grants-2002_04