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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505841Generated: October 30, 2026

4-(Hydroxymethyl)benzeneboronic acid → HCID 86653489, compound

https://huagongshe.com/reaction/1505841

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Hydroxymethyl)benzeneboronic acidHCID 2734706—
ReactantHCID 58266568HCID 58266568—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventPotassium FluorideHCID 522689—
ProductHCID 86653489HCID 86653489172.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 3-bromo-9-(2-trimethylsilanyl-ethoxymethyl)-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-6-carbonitrile (700 mg, 0.87 mmol), 4-hydroxymethylbenzeneboronic acid (400 mg, 1.32 mmol) and 1,1′-[bis(diphenylphosphino)ferrocene]dichloropalladium(II) (52.5 mg, 0.064 mmol) in acetonitrile (21 mL) and 2N aqueous potassium fluoride solution (21 mL) was divided equally across two 25 mL microwave vials. Each vial was degassed with nitrogen for 10 minutes before the mixtures were heated under microwave irradiation at 140° C. for 30 minutes. The reaction mixtures were allowed to cool to ambient temperature, combined and diluted with water (50 mL). The precipitate was collected by filtration, washed with water (50 mL) and left to air dry. The resultant grey solid was purified by flash column chromatography (silica, 40 g column, ISCO, 0-100% ethyl acetate in cyclohexane). The isolated solid was then triturated with hot t-BME to afford the title compound as a light grey solid (646 mg, 26%). LCMS (Method B): RT=4.11 min, M+H+=431.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-54133c5b0182462898f0aa0167373b85
Source noteuspto-grants-2015_12