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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529397Generated: October 27, 2026

Trifluoroacetic acid → 7-bromo-4-fluoro-2-methoxy-9H-xanthen-9-one

https://huagongshe.com/reaction/529397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBoron trifluoride etherateHCID 8000—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant5-Bromo-2-(2-fluoro-4-methoxyphenoxy)benzoic acidHCID 57475638—
SolventWaterHCID 962—
Product7-bromo-4-fluoro-2-methoxy-9H-xanthen-9-oneHCID 5747563958.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A dry 100 L glass jacketed reactor equipped with an addition funnel, reflux condenser and temperature probe was charged with 5-bromo-2-(2-fluoro-4-methoxyphenoxy)benzoic acid (2340 g, 6.9 mol). TFA (11.7 L) was carefully added to the solution followed by TFAA (1144 mL). Boron trifluoride diethyl etherate (85 mL, 0.68 mol) was then carefully added to the reaction mixture. The mixture was stirred for 4 hours at which point the reaction was transferred to another 100 L glass reactor containing 35.1 L of water cooled to 0° C. The resulting slurry was allowed to warm to RT and stir for 1 hour. The solids were filtered and washed with water (4.7 L) and 3 N NaOH (2×3.5 L) and water (7 L). The solids were transferred into a 22 L reactor and acetone (4.7 L) was added. The solids were slurried for 1.5 hour and the filtered, washing well with acetone (4.7 L). An additional slurry with acetone (6.4 L@ 45° C.) provided 1310 g of 7-bromo-4-fluoro-2-methoxy-9H-xanthen-9-one as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346827B2
Source datasetuspto-grants-2016_05
ORD IDord-c88b6a8af27d4d95baa86fa5e6d3c7d2
Source noteuspto-grants-2016_05