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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330803Generated: October 25, 2026

tert-Butyl methyl ether → (3-(5-Bromopyrimidin-2-yl)phenyl)methanol

https://huagongshe.com/reaction/330803

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methyl etherHCID 15413—
Reactant[3-(Hydroxymethyl)phenyl]boronic acidHCID 2734662—
Reactant5-Bromo-2-iodopyrimidineHCID 7006651—
ReactantTripotassium phosphate trihydrateHCID 18407952—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product(3-(5-Bromopyrimidin-2-yl)phenyl)methanolHCID 59484879—

Reaction Conditions

Temperature90 °C

Reaction Steps

750 mg (0.65 mmol) of tetrakis(triphenylphosphine)palladium are added to a solution, kept under nitrogen, of 6.11 g (21.5 mmol) of 5-bromo-2-iodo-pyrimidine, 3.91 g (25.7 mmol) of 3-(hydroxymethyl)benzeneboronic acid and 9.11 g (42.9 mmol) of tripotassium phosphate trihydrate in 120 ml of dioxane and 14 ml of water, and the mixture is stirred at 90° C. for 18 hours. The reaction mixture is cooled to room temperature, tert-butyl methyl ether and water are added, and the mixture is filtered through kieselguhr. The organic phase of the filtrate is separated off, dried over sodium sulfate and evaporated. The residue is chromatographed on a silica-gel column with dichloromethane/methanol as eluent; product: 2.49 g;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877751B2
Source datasetuspto-grants-2014_11
ORD IDord-5f83a13a72554b6d8bc07ea54d0e89dc
Source noteuspto-grants-2014_11