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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077828Generated: October 25, 2026

4-Bromotoluene → 4'-Methyl-biphenyl-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1077828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromotolueneHCID 7805—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantEthyl 3-iodobenzoateHCID 143542—
ReactantMagnesiumHCID 5462224—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product4'-Methyl-biphenyl-3-carboxylic acid ethyl esterHCID 1072875459.2%

Reaction Steps

Magnesium (1.6 g) and p-bromotoluene (10.26 g) in 60 ml of tetrahydrofuran were stirred and warmed until the reaction commenced. When the exothermic reaction had finished, the mixture was refluxed overnight. In a separate flask, 4 ml of DIBAL (1M in toluene) was added to a suspension of bis(triphenylphosphine)palladium(II) chloride (1.4 g) in 100 ml of tetrahydrofuran, followed by ethyl 3-iodobenzoate (11.04 g). To this mixture, the magnesium reagent prepared above was added dropwise, causing an exothermic reaction. The reaction mixture was stirred overnight at room temperature, and then quenched by addition of dilute hydrochloric acid. The mixture was extracted with ether, and the organic layer washed with water, and then saturated brine. The organic layer was separated, dried over sodium sulfate, the solvent evaporated under reduced pressure, and the residue chromatographed on silica gel, eluting with 5% ethyl acetate in heptane, to yield 5.69 g of ethyl 4'-methylbiphenyl-3-carboxylate, a compound of Formula (17), as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545645
Source datasetuspto-grants-1996_08
ORD IDord-35c48f52b06d4ec986257d5697e09ada
Source noteuspto-grants-1996_08