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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26756Erstellt: 25. Oktober 2026

Allyl bromide → HCID 23339063, Verbindung

https://huagongshe.com/reaction/26756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktTriethylamineHCID 8471—
EduktN-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamideHCID 162188—
LösungsmittelBenzeneHCID 241—
ProduktHCID 23339063HCID 23339063—

Reaktionsschritte

To a stirred solution of 5 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide, 3.8 parts of N,N-diethylethanamine in 200 parts of benzene are added portionwise 5 parts of 3-bromo-1-propene. After the addition is complete, the whole is heated for 21 hours at a temperature between 50°-60° C. The reaction mixture is cooled and filtered. The filtrate is washed successively with water, sodium hydrogen carbonate solution and water, dried over potassium carbonate and evaporated. The oily residue is converted into the hydrochloride salt in 1,1'-oxybisethane and 2-propanone, yielding 4 parts of N-(4-chlorophenyl)-N-[1-(2-propenyl)-4-piperidinyl]benzeneacetamide hydrochloride; mp. 225.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04151286
Quelldatensatzuspto-grants-1979_04
ORD IDord-cbff7e24092742ffa2a9ec10e70cf115
Quellennotizuspto-grants-1979_04