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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445832Generated: October 26, 2026

Methanol → 5-Hydroxy-[1,1'-biphenyl]-2-carbaldehyde

https://huagongshe.com/reaction/445832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPhenylboronic AcidHCID 66827—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Bromo-4-hydroxybenzaldehydeHCID 11084866—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product5-Hydroxy-[1,1'-biphenyl]-2-carbaldehydeHCID 57303464—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-bromo-4-hydroxybenzaldehyde (350 mg, 1.74 mmol), phenyl boronic acid (233.5 mg, 1.92 mmol), Pd(PPh3)4 (60 mg, 0.052 mmol), saturated sodium bicarbonate (6.0 mL), methanol (15 mL), and toluene (6.0 mL) was heated in a pressure tube at 120° C. overnight. Ethyl acetate and water were added and the layers separated. The aqueous phase was extracted with ethyl acetate and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (30%) to afford 5-hydroxy-[1,1′-biphenyl]-2-carbaldehyde (651).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476308B2
Source datasetuspto-grants-2013_07
ORD IDord-95808328835545a5bc47789b00b2f2db
Source noteuspto-grants-2013_07