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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541225Generated: October 25, 2026

Methyl 2-bromo-4-methylbenzoate → Methyl 2-ethyl-4-methylbenzoate

https://huagongshe.com/reaction/541225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-bromo-4-methylbenzoateHCID 21779704—
ReactantHCID 178461630HCID 178461630—
CatalystZinc bromideHCID 10421208—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-ethyl-4-methylbenzoateHCID 6828877472%

Reaction Steps

To a stirred mixture of ZnBr2 (13 g, 57.72 mmol, 2.00 equiv) in THF (230 mL) under nitrogen at 0° C. was added dropwise EtMgBr (19.5 mL, 3 M in THF). After 30 minutes at 0° C., the temperature was lowered to −78° C. and Pd(dppf)Cl2 (2 g, 2.73 mmol, 0.09 equiv) was added followed by dropwise addition of a solution of methyl 2-bromo-4-methylbenzoate (6.6 g, 28.81 mmol, 1.00 equiv) in tetrahydrofuran (200 mL). The resulting mixture was allowed to slowly reach ambient temperature and stirred under nitrogen overnight. The reaction mixture was quenched by the careful addition of 20 mL NH4Cl (aq., sat.) and extracted with 3×100 mL of ethyl acetate. The combined organic layers were washed with 1×200 mL of brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified using silica gel column chromatography with ethyl acetate/petroleum ether (1:30) as eluent to yield 3.7 g (72%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-b72143ae51a84c86b3769a1f451c8840
Source noteuspto-grants-2014_10