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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Benzyloxy-1-(tert.butyl)azetidine | HCID 20517332 | — |
| Katalysator | Nickel | HCID 935 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 1-tert-Butyl-3-hydroxyazetidine | HCID 287986 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04360464 |
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| Quelldatensatz | uspto-grants-1982_11 |
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| ORD ID | ord-d98934d06fbc49078b90b856757547a1 |
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| Quellennotiz | uspto-grants-1982_11 |
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