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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2216370Erstellt: 25. Oktober 2026

Benzyl Bromide → 2-Benzyl-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridine

https://huagongshe.com/reaction/2216370

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktMagnesiumHCID 5462224—
Edukt2-Bromo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridineHCID 21942269—
EduktHCID 178419663HCID 178419663—
KatalysatorDiphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chlorideHCID 21654969—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Benzyl-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridineHCID 21942262—

Reaktionsschritte

A mixture of 6.3 g of 2-bromo-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridine, 240 mg of 1,3-bis(diphenylphosphino)propanenickel (II) chloride and 20 ml of tetrahydrofuran was stirred in advance under nitrogen atmosphere in an ice bath. To this was added dropwise a diethyl ether solution of benzyl magnesium bromide prepared from 3.4 ml of benzyl bromide, 0.8 g of magnesium and 15 ml of diethyl ether, followed by stirring as it was at room temperature for overnight. The reaction mixture was partitioned between a saturated aqueous ammonium chloride solution and ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography with 5–10% ethyl acetate/hexane, to give 6.6 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07112593B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-7efc740474614fa8bb53d2db1bac1da8
Quellennotizuspto-grants-2006_09