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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37783Erstellt: 23. Oktober 2026

Methanol → 1-Azabicyclo[3.2.2]nonan-4-one

https://huagongshe.com/de/reaction/37783

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt3-QuinuclidinoneHCID 19507—
EduktTrimethylsilyldiazomethane hexaneHCID 86587183—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Azabicyclo[3.2.2]nonan-4-oneHCID 6420307—

Reaktionsschritte

An ice-cooled solution (5° C.) of (trimethylsilyl)diazomethane/hexane (2 N, 30 mL, 60 mmol; Aldrich) under nitrogen was treated dropwise with a solution of quinuclidin-3-one (7500 mg, 60 mmol) in dry tetrahydrofuran (40 mL). Methanol (20 mL) was added, and the yellow solution was warmed to room temperature, stirred for 24 hours, and quenched to colorless by addition of acetic acid. After a few minutes, saturated aqueous sodium carbonate (15 mL) was added. The organic layer was separated, and the aqueous solution was extracted with methylene chloride (3×50 mL). The combined organic layer and extracts were dried over magnesium sulfate, and concentrated in vacuo to give the titled compound. The material was used directly for next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524703B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-788482f2c86d4fcf85ad7c5a22fe736c
Quellennotizuspto-grants-2013_09