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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30619Generated: October 25, 2026

Sodium Carbonate → 5-Hydroxy-biphenyl-3-carbaldehyde

https://huagongshe.com/reaction/30619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant3,5-DihydroxybenzaldehydeHCID 94365—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-Hydroxy-biphenyl-3-carbaldehydeHCID 85888883—

Reaction Steps

A solution of 3,5-dihydroxybenzaldehyde (14.4 mmol) and pyridine (114 mmol) in methylene chloride (20 ml) was slowly added trifluoromethanesulfonic anhydride (36.2 mmol) keeping the temperature below 5° C. After 10 min the mixture was washed with water and the organic phase was concentrated under reduced pressure. The crude brown crystals (6.4 g—product and pyridine −1:1), phenylboronic acid (13.2 mmol), sodium carbonate (39.6 mmol) and dichlorobis(triphenylphosphine)-palladium (II). (3 mol %) was dissolved in DME (40 ml) and water (20 ml). The mixture was refluxed for 17 h under Argon, cooled to room temperature and extracted with ethyl acetate. Purification by chromatography yielded 5-Hydroxy-biphenyl-3-carbaldehyde

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423181B2
Source datasetuspto-grants-2008_09
ORD IDord-473f15d3152d4cb6b61fa8db3a5f3858
Source noteuspto-grants-2008_09