Cookies disclaimer

I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.

942-01-8 - 1,2,3,4-Tetrahydrocarbazole, 99% - B23657 - Alfa Aesar

B23657 1,2,3,4-Tetrahydrocarbazole, 99%

CAS-Nummer
942-01-8
Synonyme

Größe Preis ($) Menge Verfügbarkeit
25g 38,60
100g 103,00
Zum Warenkorb hinzufügen Zur Angebotsanfrage hinzufügen Artikel anzeigen

1,2,3,4-Tetrahydrocarbazole, 99%

MDL
MFCD00004959
EINECS
213-385-7

Chemische Eigenschaften

Formel
C12H13N
Molmasse
171.24
Schmelzpunkt
118-120°
Siedepunkt
325-330°
Löslichkeit
Insoluble in water. Solubility in methanol (almost transparency).

Anwendungen

It finds its application as a pharmaceutical intermediate and in the synthesis of aspidospermidine alkaloids.

Bemerkungen

Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.

Literaturverweise

Crosby U. Rogers and B. B. Corson. One-Step Synthesis of 1,2,3,4-Tetrahydrocarbazole and 1,2-Benzo-3,4-dihydrocarbazole.J. Am. Chem. Soc.,1947,69(11), 2910-2911.

Anahí Urrutia, et. al. Synthesis of aspidospermidine alkaloids from 1,2,3,4-tetrahydrocarbazole: Total stereoselective synthesis of (±)-18-noraspidospermidine.Tetrahedron.,2014,55(36), 11095-11108.

Deprotonation with excess superbasic n-BuLi/KO-t-Bu to give the N,ɑ-dianion has been studied in a variety of ether solvents. Formation of substantial amounts of the ɑ-ethyl derivative was observed with Et2O and THF, and also, remarkably, with various alkyl methyl ethers; e.g. in n-BuOMe, the ɑ-ethyl product was obtained in 60% yield. The ethyl group originates from the interaction of the solvent with the strong base, confirmed by the detection of ethylene in the absence of the tetrahydrocarbazole substrate: J. Org. Chem., 60, 8334 (1995). ɑ-Ethylation also occurred with 2-ethylindole, but not with 2-methyl- or 2-isopropyl analogues.

Photooxygenation with singlet oxygen, followed by reduction of the expected hydroperoxide to the allylic alcohol, is accompanied by ring contraction to a spiro ketone. The same product is formed in high yield on treatment of the spiroketone with mineral acid: J. Org. Chem., 61, 810 (1996):

GHS Gefahren- und Sicherheitshinweise

Gefahrenhinweise (EU): H303-H315-H319-H335

May be harmful if swallowed. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.

Sicherheitshinweise: P261-P280a-P305+P351+P338-P304+P340-P405-P501a

Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Weitere Referenzen

Beilstein
133771
Harmonized Tariff Code
2933.99
TSCA
No
RTECS
FE6300000

Empfohlen

Kürzlich angesehen

Chemikalien

Life science

Metalle und Stoffe

Katalysatoren

Forschungs- und Laborbedarf