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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113204Generated: October 31, 2026

Potassium Carbonate → HCID 59855502, compound

https://huagongshe.com/reaction/2113204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(4-(Dibenzo[b,d]furan-4-yl)phenyl)boronic acidHCID 59655966—
ReactantHCID 59855504HCID 59855504—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 59855502HCID 5985550272.9%

Reaction Steps

A solution of 3-(4-bromophenylmethylsulfanyl)-propanoic acid methyl ester (289 mg, 1 mmol), 4-(4-dibenzofuranyl)benzeneboronic acid (302 mg, 1.05 mmol) and Pd(PPh3)4 (52 mg, 5 mol %) in toluene (10 mL) and ethanol (3.0 mL) was treated with 2 M K2CO3 (1.5 mL). The reaction mixture was heated to reflux for 2 h, cooled to room temperature, diluted with ethyl acetate (100 mL). The organic layer was washed successively with 2% aq HCl and sat. aq NaCl, dried over MgSO4 and concentrated. Purification by flash column chromatography (2-10% ethyl acetate in heptane) gave 3-(4′-dibenzofuran-4-yl-biphen-4-ylmethylsulfanyl)-propanoic acid methyl ester (330 mg, 72%) as white solid. 1H NMR (CDCl3), 8.01 (d, J=8 Hz, 2H), 7.94 (d, J=8 Hz, 2H), 7.78 (d, J=8 Hz, 2H), 7.66 (m, 4H), 7.42 (m, 5H), 3.81 (s, 2H), 3.71 (s, 3H), 2.76 (t, J=6 Hz, 2H), 2.56 (t, J=6 Hz, 2H). LCMS 475 (M++23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524878B2
Source datasetuspto-grants-2009_04
ORD IDord-9ece016d2fba49afb61fe26f10c4879b
Source noteuspto-grants-2009_04