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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496939Generated: October 26, 2026

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

https://huagongshe.com/reaction/496939

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 numberUS06946560B2
Source datasetuspto-grants-2005_09
ORD IDord-5d8f8aee9b8d4bb5bec7277d32eb98d2
Source noteuspto-grants-2005_09