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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 461559Erstellt: 24. Oktober 2026

Hydrochloric Acid → 3-(Dimethylamino)-7-methoxy-1,2,3,4-tetrahydrocarbazole

https://huagongshe.com/de/reaction/461559

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-(Dimethylamino)cyclohexan-1-oneHCID 138887—
Edukt3-Methoxyphenylhydrazine hydrochlorideHCID 2723940—
LösungsmittelEthanolHCID 702—
Produkt3-(Dimethylamino)-7-methoxy-1,2,3,4-tetrahydrocarbazoleHCID 12361840—

Reaktionsschritte

A solution of 7 g. of dimethylaminocyclohexanone and 8.4 g. of 3-methoxyphenylhydrazine hydrochloride in 40 ml. of absolute ethyl alcohol and 12 ml. of 4-N hydrogen chloride in ethyl alcohol was heated under reflux for two hours. The reaction mixture was allowed to stand for sixteen hours, filtered, and the filtrate was evaporated to dryness under reduced pressure. The residue was taken up in water, made alkaline with dilute sodium hydroxide and extracted with ether. The ether extract was washed with water, dried, ethereal hydrogen chloride was added, and the resulting oily precipitate was collected by decantation, recrystallized twice from isopropyl alcohol, suspended in chloroform and treated with dilute sodium hydroxide. The chloroform extract was evaporated to dryness under reduced pressure to give 3-(dimethylamino)-7-methoxy-1,2,3,4-tetrahydrocarbazole, m.p. 100°-105° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04062864
Quelldatensatzuspto-grants-1977_12
ORD IDord-de677e1a6ce8451ea6d3c1aaf616332d
Quellennotizuspto-grants-1977_12