Reaktion #615

ord-cb0ae83e039e422babb6d81e64a4df69

Reaktionsgleichung

Brc1ccc(Br)cc1
Brc1ccc(Br)cc1
COC(=O)C1CCNC1
COC(=O)C1CCNC1
COC(=O)C1CCN(c2ccc(Br)cc2)C1
COC(=O)C1CCN(c2ccc(B
Ausbeute 29.1%

Lösungsmittel

Reaktionsbedingungen

Temperatur
85°CELSIUS

Vorschrift

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.

Quelle

750 AstraZeneca ELN dataset