Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26749Erstellt: 25. Oktober 2026

Allyl bromide → N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine

https://huagongshe.com/reaction/26749

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktTriethylamineHCID 8471—
EduktN-(4-chlorophenyl)piperidin-4-amineHCID 7183033—
LösungsmittelBenzeneHCID 241—
ProduktN-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamineHCID 23339007—

Reaktionsschritte

To a stirred mixture of 15 parts of N-(4-chlorophenyl)-4-piperidinamine, 12 parts of N,N-diethylethanamine in 130 parts of benzene is added dropwise a solution of 10.3 parts of 3-bromo-1-propene in 70 parts of benzene. Upon completion, the whole is stirred first for 20h.30 at room temperature and further for 40 minutes at reflux. The reaction mixture is cooled, filtered and the filtrate is evaporated. The residue is taken up in 1,1'-oxybisethane and treated with activated charcoal. The latter is filtered off and the 1,1'-oxybisethane is evaporated again, yielding 2.9 parts of N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine; mp. 90° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04151286
Quelldatensatzuspto-grants-1979_04
ORD IDord-d72e82e1e56f4241b4c164d2fa7acc77
Quellennotizuspto-grants-1979_04