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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892084Generated: November 1, 2026

Toluene → Methyl 5-(4-phenylphenyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/1892084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant1,1'-Biphenyl-4-yl-boronic acidHCID 151253—
ReactantMethyl 5-bromothiophene-2-carboxylateHCID 605713—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductMethyl 5-(4-phenylphenyl)thiophene-2-carboxylateHCID 1231796575.2%

Reaction Steps

A mixture of compound 1021 (5.0 g, 22.6 mmol), biphenyl-4-ylboronic acid (5.4 g, 27.1 mmol), sodium carbonate (5.9 g, 56.5 mmol), tetrakis(triphenylphosphine)palladium(0) (2.65 g, 2.3 mmol), toluene (200 mL), ethanol (100 mL) and water (50 mL) was heated to reflux for 12 hours under nitrogen atmosphere. The reaction mixture was cooled to ambient temperature, and extracted with dichloromethane (2×250 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. The residue was purified by flash chromatography with silica gel (5% EtOAc in hexane) to give compound 1022 (5.0 g). 1H NMR (CDCl3, 300 MHz) δ 3.92 (s, 3H), 7.32-7.49 (m, 4H), 7.62-7.80 (m, 7H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507647B2
Source datasetuspto-grants-2013_08
ORD IDord-82caae39f2b942b092f05e988f10f05f
Source noteuspto-grants-2013_08