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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 586628Erstellt: 25. Oktober 2026

p-Chlorophenacyl bromide → 6-(4-chlorophenyl)-7-phenyl-2,3-dihydro-1H-pyrrolizine

https://huagongshe.com/reaction/586628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Chlorophenacyl bromideHCID 68303—
Edukt5-benzyl-3,4-dihydro-2H-pyrroleHCID 224018—
EduktSodium BicarbonateHCID 516892—
LösungsmittelMethanolHCID 887—
Produkt6-(4-chlorophenyl)-7-phenyl-2,3-dihydro-1H-pyrrolizineHCID 997165656%

Reaktionsschritte

(according to Laufer et al. J. Med. Chem. 1994, 37, 1894-1897) 2-Benzyl-1-pyrroline (Example 1 a, 19.8 g, 80% strength, 0.1 mol), dissolved in MeOH (300 ml) is treated with 4-chlorophenacyl bromide (23,4 g, 0.1 mol) and then with NaHCO3 (10 g, 0.12 mol) and stirred at RT for 16 h with exclusion of light. Precipitated crystallizate is filtered off with suction and washed with MeOH. 16.4 g (56%) of product are obtained after drying.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06936632B2
Quelldatensatzuspto-grants-2005_08
ORD IDord-b702cea50b074740a8db945044aa7d56
Quellennotizuspto-grants-2005_08