HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36093Erstellt: 23. Oktober 2026
(2S-trans)-2,3-bis[(benzyloxy)methyl]cyclobutanone → Dibenzyl ether
https://huagongshe.com/de/reaction/36093
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | (2S-trans)-2,3-bis[(benzyloxy)methyl]cyclobutanone | HCID 14863583 | — |
| Edukt | Triisobutylaluminum | HCID 16682931 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | Dibenzyl ether | HCID 7657 | — |
Reaktionsschritte
A solution of (2S-trans)-2,3-bis[(benzyloxy)methyl]cyclobutanone (0.2 g., 0.645 mmole) in toluene (4 ml.) was added dropwise over 10 minutes to a solution of triisobutylaluminum (0.91 M in hexane, 0.9 ml., 0.816 mmole) in toluene (2 ml.) at -40° C. The mixture was stirred at -50° C. for 4 hours and at -40° C. for one hour. A solution of triisobutylaluminum (1 ml., 0.91 mmole) was added to the reaction mixture. After stirring for 30 minutes the reaction was quenched by adding 10% hydrochloric acid (2 ml.) at -40° C. The organic phase was washed with brine, dried (magnesium sulfate), and the solvent was evaporated to give [1S-(1α,2β,3β)]-3-hydroxy-1,2-cyclobutanedimethanol, dibenzyl ether; TLC (30% ethyl acetate/hexane) Rf =0.3. The product contained about 5% of the isomeric compound; TLC (30% ethyl acetate/hexane) Rf =0.2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05412134 |
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| Quelldatensatz | uspto-grants-1995_05 |
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| ORD ID | ord-4dfa1debe66d46a791cd9e5f90acd2c9 |
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| Quellennotiz | uspto-grants-1995_05 |
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