Perchloric Acid → 1-azabicyclo-[2,2,2]-octan-3-carboxaldehyde O-methyloxime

HRID 2081237Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2081237
Cl(O)(=O)(=O)=O.CO[CH:8]=[C:9]1[CH:14]2[CH2:15][CH2:16][N:11]([CH2:12][CH2:13]2)[CH2:10]1.Cl.[O:18]([NH2:20])[CH3:19]>C(Cl)(Cl)Cl.O.CO>[CH3:19][O:18][N:20]=[CH:8][CH:9]1[CH:14]2[CH2:13][CH2:12][N:11]([CH2:16][CH2:15]2)[CH2:10]1

Komponenten

7

Edukt 3

HCID 24247Perchloric AcidHCID 521874O-Methylhydroxylamine hydrochlorideHCID 537726003-Methoxy methylidene quinuclidine

Produkt 1

HCID 542801241-azabicyclo-[2,2,2]-octan-3-carboxaldehyde O-methyloxime

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittelHCID 6212ChloroformLösungsmittel

Versuchsvorschrift

11 cm3 of a 70% aqueous solution of perchloric acid is added at ambient temperature to 4.6 g of 3-methoxy methylidene quinuclidine (Heterocycles 244, 4-971 (1986)) in solution in 46 cm3 of chloroform. After one hour of contact, 2.5 g of methoxylamine hydrochloride in 10 cm3 of water and 10 cm3 of methanol is added and the reaction medium is maintained in this way for one night, and is then concentrated, alkalized with 2N sodium hydroxide, extracted with ethyl acetate; the solvents are evaporated, and the residue is taken up in ethyl ether and filtered. The filtrate is distilled at 150° C. under 0.08 mbar and 3.2 g of expected product is obtained.

Aufarbeitung

  1. temperaturethe reaction medium is maintained in this way for one night
  2. concentrationis then concentrated
  3. extractionextracted with ethyl acetate
  4. customthe solvents are evaporated
  5. filtrationfiltered
  6. distillationThe filtrate is distilled at 150° C. under 0.08 mbar

Quellen und Nachweise

ORD-Eintrag
ord-c03419fc618d48aabc0828509c06dade
Quelldatensatz
uspto-grants-1993_02
Patentnummer
US05183893

Notizen zur Reaktion

Wird geladen…