Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795655Generated: October 31, 2026

Phenylboronic Acid → (1,1'-Biphenyl)-2-methanol

https://huagongshe.com/reaction/1795655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
Reactant2-Bromobenzyl alcoholHCID 72850—
ReactantPotassium FluorideHCID 522689—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Product(1,1'-Biphenyl)-2-methanolHCID 7622983%

Reaction Steps

An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.02 mmol, 2.0 mol %), phenylboronic acid (183 mg, 1.5 mmol), potassium fluoride (174 mg, 3.0 mmol), and 2-bromobenzyl alcohol (187 mg, 1.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) was added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at room temperature until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL), filtered througth celite, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 153 mg (83%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026498B2
Source datasetuspto-grants-2006_04
ORD IDord-34a59d9997214a7ba70361dc80d3beda
Source noteuspto-grants-2006_04