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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromotoluene | HCID 7805 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Ethyl 3-iodobenzoate | HCID 143542 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-Methyl-biphenyl-3-carboxylic acid ethyl ester | HCID 10728754 | 59.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05545645 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-35c48f52b06d4ec986257d5697e09ada |
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| Source note | uspto-grants-1996_08 |
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