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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455552Generated: October 30, 2026

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

https://huagongshe.com/reaction/455552

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 followed by TFAA (1144 mL). Boron trifluoride diethyl etherate (85 mL, 0.68 mol) was then carefully added. Stirring was continued to 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 numberUS08497264B2
Source datasetuspto-grants-2013_07
ORD IDord-c99fa03359054e6688e1e176ed2c3718
Source noteuspto-grants-2013_07