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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726384Generated: October 26, 2026

Sodium Carbonate → Methyl 3-bromo-5-(4-fluorophenyl)benzoate

https://huagongshe.com/reaction/1726384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Fluorophenylboronic acidHCID 285645—
ReactantMethyl 3,5-DibromobenzoateHCID 621923—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthanolHCID 702—
SolventDiglymeHCID 8150—
ProductMethyl 3,5-di(4-fluorophenyl)benzoateHCID 690620424%
ProductMethyl 3-bromo-5-(4-fluorophenyl)benzoateHCID 6906841823%

Reaction Conditions

Temperature88 °C

Reaction Steps

To a solution of methyl 3,5-dibromobenzoate (3.00 g, 10.2 mmol) and 4-fluoro-phenyl boronic acid (1.43 g, 10.2 mmol) in 2-methoxyethyl ether (60 ml) and ethanol (3 ml) was added Na2CO3 (saturated, 9 ml), followed by tetrakis(triphenylphosphine) palladium (0) (0.2 g). The mixture was heated at 88° C. for 1.5 h, then cooled to room temperature, partitioned between hexane and water, and the organic phase washed with brine, dried over anhydrous sodium sulfate, decanted, and the organic solution concentrated under reduced pressure. The residue was purified by silica gel chromatography (1% EtOAc in hexane) to yield methyl 3-bromo-5-(4-fluorophenyl)benzoate (intermediate XXXIVa, 0.725 g, 23%) as a white solid, and methyl 3,5-di(4-fluorophenyl)benzoate (intermediate XXXIVb, 0.128 g, 4%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491821B2
Source datasetuspto-grants-2009_02
ORD IDord-f7d2824e37d748efbaa5e49b5eac6485
Source noteuspto-grants-2009_02