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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216282Generated: October 31, 2026

Methyl 4-bromobenzoate → Methyl Benzoate

https://huagongshe.com/reaction/2216282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-bromobenzoateHCID 12081—
Reactant1,4-DioxaneHCID 31275—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-(2-Methoxyethyl)piperazineHCID 2734638—
SolventEthyl AcetateHCID 8857—
ProductMethyl BenzoateHCID 7150—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 10 ml of 1,4-dioxan is added 0.645 g (3.0 mmol) of methyl-4-bromobenzoate 0.519 g (3.6 mmol) of 1-(2-methoxy-ethyl-piperazine, 0.892 g (8.47 mmol) of potassium phosphate, 0.177 g (0.45 mmol) of 2-dicycohexylphosphino-2′-(N,N-dimethylamino)biphenyl and 0.137 g (0.15 mmol) tris-(benzylideneacetone)palladium (0). The resulting reaction mixture is stirred under argon for 5 hours at 100° C., then cooled to room temperature, diluted with ethyl acetate and filtered. The filtrate is washed once with H2O and once with brine, the organic layer separated and dried over Na2SO4. Purification of the crude product by flash chromatography (dichloromethane/methanol) yields 0.52 g of 4-[4-(2-methoxy-ethyl)-piperazin-1-yl)]benzoic acid methyl ester as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112589B2
Source datasetuspto-grants-2006_09
ORD IDord-eb71949554154dd0ac8446d9f681a659
Source noteuspto-grants-2006_09