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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600934Generated: October 31, 2026

Water → (2R)-1-(3'-Aminobiphenyl-4-yloxy)-4-(3-pyridyl)-2-butanol

https://huagongshe.com/reaction/1600934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant3-Aminophenylboronic acid monohydrateHCID 14389423—
Reactant(2R)-1-(4-bromophenoxy)-4-(3-pyridyl)-2-butanolHCID 53756856—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product(2R)-1-(3'-Aminobiphenyl-4-yloxy)-4-(3-pyridyl)-2-butanolHCID 5400680782.9%

Reaction Steps

Aqueous sodium carbonate solution (2 M, 1.55 ml) was added to a solution of (2R)-1-(4-bromophenoxy)-4-(3-pyridyl)-2-butanol (0.50 g), 3-aminobenzeneboronic acid monohydrate (0.26 g) and tetrakis(triphenylphosphine)palladium(0) (0.045 g) in ethanol (1.72 ml) and toluene (6.9 ml). The mixture was stirred at reflux under a nitrogen atmosphere for 3 hours and then, cooled to room temperature. The reaction mixture was poured into water and then extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography over silica eluting with dichloromethane:methanol (19:1) to give the title compound (0.43 g) as an which was recrystallised from isohexane:ethyl acetate to give a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977105
Source datasetuspto-grants-1999_11
ORD IDord-a600fa305fcd4355b87616b37b915bd4
Source noteuspto-grants-1999_11