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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175591Generated: October 31, 2026

Water → 2-Methyl-2-(4-(pyrimidin-5-yl)phenyl)propanoic acid

https://huagongshe.com/reaction/1175591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(Pyrimidin-5-yl)boronic acidHCID 2795193—
Reactant2-(4-Bromophenyl)-2-methylpropanoic acidHCID 10933679—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium HydroxideHCID 14798—
Product2-Methyl-2-(4-(pyrimidin-5-yl)phenyl)propanoic acidHCID 6877724974%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-(4-Bromophenyl)-2-methylpropanoic acid (5.71 g, 23.5 mmol) was dissolved in DME (140 mL) and water (35 mL) and pyrimidin-5-ylboronic acid (2.92 g, 23.5 mmol) and potassium carbonate (11.4 g, 82.2 mmol) were added to the solution. The mixture was degassed using an argon stream, and Pd(PPh3)4 (1.35 g, 1.17 mmol) was added. The mixture was heated (80° C.) under argon overnight then cooled to room temperature. The solution was diluted with 1M NaOH (20 mL) and washed with EtOAc. The aqueous phase was acidified with 6N aq. HCl to pH 4-5 and extracted with EtOAc (3×). The combined extract was successively washed with water and brine, dried over MgSO4, filtered and evaporated to yield 4.2 g (74%) of the crude 2-Methyl-2-(4-(pyrimidin-5-yl)phenyl)propanoic acid (MS+H, 243) that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842324B2
Source datasetuspto-grants-2010_11
ORD IDord-b0374616427546a294036c938abf74aa
Source noteuspto-grants-2010_11