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HRID 461560Erstellt: 24. Oktober 2026

Methanesulfonic Acid → 3-(1-Piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazole

https://huagongshe.com/de/reaction/461560

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonic AcidHCID 6395—
Edukt(2,4-Difluoro-phenyl)-hydrazineHCID 588958—
EduktCyclohexanone, 4-(1-piperidinyl)-HCID 12361785—
LösungsmittelEthanolHCID 702—
Produkt3-(1-Piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazoleHCID 12361824—

Reaktionsschritte

A solution of 10.2 g. of 4-(1-piperidyl)-cyclohexanone, 8.1 g. of 2,4-difluorophenylhydrazine, and 11 g. of methanesulfonic acid in 100 ml. of absolute ethyl alcohol was heated under reflux for 12 hours, cooled, filtered, and the filtrate was evaporated to dryness under reduced pressure. The residue was treated in ether with 10% potassium hydroxide solution and the ether extract was washed with water, dried, and treated with hydrogen chloride in ethyl alcohol (excess HCl was avoided). The resulting gummy precipitate was separated by decantation and suspended in boiling isopropyl alcohol. The hot mixture was filtered to give, after recrystallization from absolute ethyl alcohol, 4.5 g. of 3-(1-piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazole hydrochloride, m.p. > 290° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04062864
Quelldatensatzuspto-grants-1977_12
ORD IDord-babb356db7d24e0ebcc7209ba8042f2f
Quellennotizuspto-grants-1977_12