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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 519Erstellt: 23. Oktober 2026

1,4-Dibromobenzene → Methyl 1-(4-bromophenyl)pyrrolidine-3-carboxylate

https://huagongshe.com/de/reaction/519

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DibromobenzeneHCID 7804—
EduktMethyl Pyrrolidine-3-carboxylateHCID 4114360—
ReagenzSodium t-butoxideHCID 23676156—
KatalysatorBinap, (A+-)-HCID 634876—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
ProduktMethyl 1-(4-bromophenyl)pyrrolidine-3-carboxylateHCID 8398169329,15%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

A suspension of methyl pyrrolidine-3-carboxylate (800 mg, 6.19 mmol), 1,4-dibromobenzene (1461 mg, 6.19 mmol), TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (142 mg, 0.15 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (289 mg, 0.46 mmol) and Sodium Tert-Butoxide (714 mg, 7.43 mmol) in anhydrous toluene (30 mL) was stirred at 85 °C under nitrogen for 4 hours. The reaction was cooled to ambient temperature, diluted with Ether (100 mL) and filtered through celite. The filtrate was evaporated in vacuo to yield crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in heptane. Pure fractions were evaporated to dryness to afford methyl 1-(4-bromophenyl)pyrrolidine-3-carboxylate (513 mg, 29.1 %) as a yellow solid.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-cb0ae83e039e422babb6d81e64a4df69
Quellennotiz750 AstraZeneca ELN dataset