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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2198854Erstellt: 26. Oktober 2026

3-Benzyloxy-1-(tert.butyl)azetidine → 1-tert-Butyl-3-hydroxyazetidine

https://huagongshe.com/reaction/2198854

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Benzyloxy-1-(tert.butyl)azetidineHCID 20517332—
KatalysatorNickelHCID 935—
LösungsmittelEthanolHCID 702—
Produkt1-tert-Butyl-3-hydroxyazetidineHCID 28798676%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A solution of 4.4 parts of 3-benzyloxy-1-(tert.-butyl)azetidine in 30 parts of ethanol was added to an autoclave together with 2 parts of Raney nickel as catalyst. Under a hydrogen gas pressure of 100 atmospheres, the mixture was stirred at 40° C. for 15 hours to perform the reduction. The catalyst was separated by filtration, and the remaining ethanol solution was concentrated to dryness. The resulting oily substance was dissolved in n-hexane and cooled. As a result 2.0 parts of 1-(tert.butyl)-3-azetidinol melting at 42°-43° C. The yield was 76%. The results of infra-red spectrum analysis and nuclear magnetic resonance analysis of the product are as follows:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04360464
Quelldatensatzuspto-grants-1982_11
ORD IDord-d98934d06fbc49078b90b856757547a1
Quellennotizuspto-grants-1982_11