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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16785Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 4-bromobenzoateHCID 12081—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt1-AcetylpiperazineHCID 83795—
Edukt2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
LösungsmittelTolueneHCID 1140—
ProduktMethyl 4-(4-acetylpiperazin-1-yl)benzoateHCID 5744040956,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737149B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-743a010bd61e44b484bd996ac6892806
Quellennotizuspto-grants-2010_06