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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425272Generated: October 30, 2026

Boron trifluoride etherate → 3-Bromo-9H-xanthen-9-one

https://huagongshe.com/reaction/425272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromo-2-phenoxybenzoic acidHCID 23053920—
SolventDichloromethaneHCID 6344—
Product3-Bromo-9H-xanthen-9-oneHCID 23160896.7%

Reaction Steps

To a suspension of 4-bromo-2-phenoxy-benzoic acid (35.1 g, 120 mmol) in CH2Cl2 (350 mL) at 0° C. was added trifluoroacetic anhydride (20.3 mL, 144 mmol), dropwise, and the reaction was stirred for 15 min. At that time, boron trifluoride diethyl etherate (1.46 mL, 12.0 mmol) was added, dropwise. The reaction became homogeneous upon stirring for 1 h at room temperature. Upon completion, the reaction was poured into 1 N NaOH, and the organic phase was dried over magnesium sulfate, filtered, and concentrated to give Compound 3a (32.14 g, 116 mmol). MS m/z (MH+) 275.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106207B2
Source datasetuspto-grants-2012_01
ORD IDord-7c50d6b1737843ad92a98d52f4561fec
Source noteuspto-grants-2012_01