HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541268Generated: November 1, 2026
Methyl 4-bromo-2-methylbenzoate → Benzoic acid, 4-ethyl-2-methyl-, methyl ester
https://huagongshe.com/reaction/541268
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-bromo-2-methylbenzoate | HCID 22031226 | — |
| Reactant | HCID 178461630 | HCID 178461630 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzoic acid, 4-ethyl-2-methyl-, methyl ester | HCID 10773666 | 84% |
Reaction Steps
To a stirred mixture of ZnBr2 (4.50 g, 20.0 mmol, 2.00 equiv) in tetrahydrofuran (50 mL) under nitrogen at 0° C. was added EtMgBr (6.6 mL, 2.00 equiv, 3M in THF) dropwise. After stiffing for 30 min at 0° C., the temperature was lowered to −78° C. and Pd(dppf)Cl2 (1.08 g, 1.48 mmol, 0.30 equiv) was added followed by a solution of methyl 4-bromo-2-methylbenzoate (compound 152.1, 2.30 g, 10.0 mmol, 1.00 equiv) in tetrahydrofuran (20 mL). The resulting mixture was stirred for 30 min at −78° C., warmed to room temperature, and stirred overnight. The reaction mixture was carefully quenched with 60 mL of NH4Cl (aq.) and extracted with 3×50 mL of ethyl acetate. The combined organic phases were dried (Na2SO4) and concentrated in vacuo. The residue was purified using silica gel column chromatography with ethyl acetate/petroleum ether (1:100-1:5) as eluent to furnish 1.50 g (84%) of methyl 4-ethyl-2-methylbenzoate as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871790B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-c77f85d1b8f34dbfb38436ed1d7afa69 |
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| Source note | uspto-grants-2014_10 |
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