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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16785Generated: October 23, 2026

Methyl 4-bromobenzoate → Methyl 4-(4-acetylpiperazin-1-yl)benzoate

https://huagongshe.com/en/reaction/16785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-bromobenzoateHCID 12081—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-AcetylpiperazineHCID 83795—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
SolventTolueneHCID 1140—
ProductMethyl 4-(4-acetylpiperazin-1-yl)benzoateHCID 5744040956.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A deoxygenated suspension of 1-acetylpiperazine (0.308 g, 2.40 mmol), methyl 4-bromobenzoate (0.430 g, 2 mmol), tri-potassium orthophosphate (0.594 g, 2.80 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (0.164 g, 0.40 mmol) and tris(dibenzylideneacetone)dipaladium(0) (0.092 g, 0.10 mmol) in toluene (10 mL) was stirred at 100° C., over a period of 24 h under nitrogen. The cooled reaction mixture was filtered and evaporated to give crude product. The crude product was purified by silica column chromatography, eluting with a gradient 0-5% MeOH in DCM. Pure fractions were evaporated to dryness to afford methyl 4-(4-acetylpiperazin-1-yl)benzoate (0.295 g, 56.2%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737149B2
Source datasetuspto-grants-2010_06
ORD IDord-743a010bd61e44b484bd996ac6892806
Source noteuspto-grants-2010_06