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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-bromo-2-methylbenzoateHCID 22031226—
ReactantHCID 178461630HCID 178461630—
CatalystZinc bromideHCID 10421208—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTetrahydrofuranHCID 8028—
ProductBenzoic acid, 4-ethyl-2-methyl-, methyl esterHCID 1077366684%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-c77f85d1b8f34dbfb38436ed1d7afa69
Source noteuspto-grants-2014_10