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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 917945Erstellt: 26. Oktober 2026

Toluene → 5-(3-Chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepine

https://huagongshe.com/reaction/917945

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
Edukt1-Bromo-3-chloropropaneHCID 8006—
EduktIminodibenylHCID 10308—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelHexaneHCID 8058—
Produkt5-(3-Chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepineHCID 286779—

Reaktionsschritte

A solution of 10,11-dihydro-5H-dibenz[b,f]azepine (19.5 gms.; 0.10 moles) in dry ether was added to a solution of 7.7 gms. (0.12 mole) of butyl lithium in hexane. The stirred solution was warmed for approximately one hour and then 31.0 gms. (0.20 mole) of bromopropylchloride in ether was added and the resulting mixture heated at reflux for 16 hours. Aliquot analysis showed no reaction had taken place. Approximately one liter of toluene was added to the reaction mixture, lower boiling solvents were removed by distillation and the reaction mixture heated at reflux with stirring for 12 hours. On working up the reaction mixture, there was obtained 7.0 gms. of 5-(3-chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepine which distilled at 150°-153°C. (0.03 mm.). An additional 6.0 gms. of impure material which contained approximately 15% of unreacted 10,11-dihydro-5H-dibenz[b,f]azepine was obtained which distilled at 140°-150°C. (0.03 mm.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03968217
Quelldatensatzuspto-grants-1976_07
ORD IDord-4d3f62cca67a4663aab24141d04cde36
Quellennotizuspto-grants-1976_07