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HRID 27426Erstellt: 23. Oktober 2026

2H-Azepine, 3,4,5,6-tetrahydro-7-methoxy- → 2-(alpha-Cyano-4-chlorobenzylidene)perhydroazepine

https://huagongshe.com/de/reaction/27426

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2H-Azepine, 3,4,5,6-tetrahydro-7-methoxy-HCID 75657—
Edukt4-Chlorobenzyl cyanideHCID 241582—
EduktDiazabicyclo[5.4.0]undec-5-eneHCID 22258625—
LösungsmittelMethanolHCID 887—
Produkt2-(alpha-Cyano-4-chlorobenzylidene)perhydroazepineHCID 7059504267,6%

Reaktionsschritte

Agitate a mixture of 5.0 g of 4-chlorobenzyl cyanide, 5.5 g of caprolactim methyl ether and 0.5 g of diazabicyclo [5.4.0]undec-5-ene under nitrogen for 18 hours at 125°. Cool the thus-obtained reaction mixture to ambient temperature and then rub down the crystallizing residue with 20 ml of methyl alcohol before filtering to obtain 5.5 g of the title compound. Recrystallize this compound from methyl alcohol to obtain a product with a MP of 114° to 117°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04221788
Quelldatensatzuspto-grants-1980_09
ORD IDord-34ac4d4d324f4803aaa661b56366f157
Quellennotizuspto-grants-1980_09