Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091816Generated: November 1, 2026

Potassium Phosphate, Tribasic → Methyl 3-bromo-5-(5-methylpyridin-2-yl)benzoate

https://huagongshe.com/reaction/2091816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Bromo-5-methylpyridineHCID 564216—
ReactantMethyl 3-bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)benzoateHCID 53436914—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 3-bromo-5-(5-methylpyridin-2-yl)benzoateHCID 5959970451.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-bromo-5-methyl-pyridine (10.27 g, 59.68 mmol) and palladium tetrakis(triphenylphosphine) (1.88 g, 1.65 mmol) in 300 mL DME was stirred at 60° C. under nitrogen for 30 minutes. To this mixture was added 3-bromo-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzoic acid methyl ester (18.5 g, 54.25 mmol), followed by K3PO4 23.03 g, 108.5 mmol) in 40 mL water. The mixture was refluxed for eight hours, then cooled to room temperature and partitioned between water and EtOAc. The combined organic layers were washed with water, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified via flash chromatography (5:1 EtOAc/hexanes) to give 8.5 g of 3-bromo-5-(5-methyl-pyridin-2-yl)-benzoic acid methyl ester, MS (M+H)=306.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440673B2
Source datasetuspto-grants-2013_05
ORD IDord-65d42f6c25ed4ad88312dce7ffd46e45
Source noteuspto-grants-2013_05