Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234147Generated: October 30, 2026

1,1'-Biphenyl-4-yl-boronic acid → HCID 66760170, compound

https://huagongshe.com/reaction/2234147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-Biphenyl-4-yl-boronic acidHCID 151253—
ReactantPotassium FluorideHCID 522689—
Reactant{4-[3,3-Bis-(4-bromo-phenyl)-allylsulfanyl]-2-methyl-phenoxy}-acetic acidHCID 10370262—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystHCID 178418851HCID 178418851—
ProductHCID 66760170HCID 66760170—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of {4-[3,3-bis-(4-bromo-phenyl)-allylsulfanyl]-2-methyl-phenoxy}-acetic acid (example 1) (225 mg, 0.410 mmol), 4-biphenylboronic acid (163 mg, 0.82 mmol), KF (79 mg, 1.35 mmol), Pd2(dba)3 (23 mg, 0.025 mmol) and Pd(P(t-Bu)3)2 (25 mg, 0.049 mmol) was evacuated for air and kept under nitrogen. THF (6 ml) was added and the reaction mixture was stirred at 70° C. overnight. A saturated aqueous NH4Cl (5 ml) solution was added, and the mixture was extracted with methylene chloride (2×20 ml). The combined organic phases were dried an evaporated. The isolated products were further purified on column chromatography using methylene chloride:THF (40:1) as eluent. The isolated products were further purified on HPLC using acetonitril:water (7:3) increasing to pure acetonotril as eluent. The title product was isolated as an E/Z mixture in 40 mg (16%) yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709528B2
Source datasetuspto-grants-2010_05
ORD IDord-635bc1c25b104fe6ad70c45a92ae8053
Source noteuspto-grants-2010_05