Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 976288Erstellt: 24. Oktober 2026

1,2-Dimethoxyethane → 1-Azabicyclo(2.2.2)octane-3-carbonitrile

https://huagongshe.com/de/reaction/976288

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DimethoxyethaneHCID 8071—
Edukt3-QuinuclidinoneHCID 19507—
Edukt1-Isocyanatomethanesulfonyl-4-methylbenzeneHCID 11789078—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelEthanolHCID 702—
Produkt1-Azabicyclo(2.2.2)octane-3-carbonitrileHCID 14286574,5%

Reaktionsschritte

A solution of potassium tert-butoxide (18.27 ml) in 1:1 (v/v) mixture of dimethoxyethane and ethanol (100 ml) was added slowly to a stirred mixture of 3-quinuclidinone (8.14 g), tosylmethylisocyanate (16.53 g) in dry ethanol (6.5 ml), and dry dimethoxyethane (228 ml) under an atmosphere of argon whilst maintaining the temperature below 10° C. The reaction mixture was allowed to warm to ambient temperature and stirred at this temperature for 30 minutes. The reaction mixture was then stirred at 40° C. for 3 hours. The reaction mixture was cooled, filtered and the filtrate evaporated. The residue was purified by flash column chromatography on alumina (Brockmann Grade I) using a 2:98 (v/v) mixture of methanol/ethyl acetate as eluant to give 3-cyanoquinuclidine (6.6 g), microanalysis, found: C, 67.6; H, 8.5; N, 18.7%; C8H12N2 requires: C, 70.6; H, 8.8; N, 20.6%; NMR (CDCl3): 1.4-1.7 (3H, m), 1.85-2.0 (1H, m) 2.0-2.1 (1H, m) and 2.6-3.4 (7H, m); m/z 137 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05612352
Quelldatensatzuspto-grants-1997_03
ORD IDord-674cbd93d49343d395987c36d51fabd6
Quellennotizuspto-grants-1997_03