HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 461560Erstellt: 24. Oktober 2026
Methanesulfonic Acid → 3-(1-Piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazole
https://huagongshe.com/de/reaction/461560
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanesulfonic Acid | HCID 6395 | — |
| Edukt | (2,4-Difluoro-phenyl)-hydrazine | HCID 588958 | — |
| Edukt | Cyclohexanone, 4-(1-piperidinyl)- | HCID 12361785 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 3-(1-Piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04062864 |
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| Quelldatensatz | uspto-grants-1977_12 |
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| ORD ID | ord-babb356db7d24e0ebcc7209ba8042f2f |
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| Quellennotiz | uspto-grants-1977_12 |
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