HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1196213Erstellt: 24. Oktober 2026
Boron trifluoride etherate → (3S,4S)-4-(1-(R)-hydroxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone
https://huagongshe.com/de/reaction/1196213
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Boron trifluoride etherate | HCID 8000 | — |
| Edukt | 1,3-Dimethoxybenzene | HCID 9025 | — |
| Edukt | (3S,4R)-4-(1-(R)-t-butyldimethylsilyloxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone | HCID 67798445 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (3S,4S)-4-(1-(R)-hydroxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone | HCID 13960427 | — |
Reaktionsschritte
To a solution of (3S,4R)-4-(1-(R)-t-butyldimethylsilyloxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone (20 g) in dry dichloromethane (200 ml) were added 1,3-dimethoxybenzene (7.8 g) and boron trifluoride etherate (23 g) at 10 °-20° C., and the resultant mixture was stirred at room temperature for 3 hours, followed by heating under reflux for 3-5 hours. The reaction mixture was cooled down to 10°-15° C., washed successively with brine (200 ml×2), 2.5% sodium bicarbonate (200 ml) and brine (200 ml) and dried over anhydrous sodium sulfate. Filtration and concentration of the filtrate in vacuo gave an oily residue which was purified by silica gel chromatography to yield (3S,4S)-4-(1-(R)-hydroxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05112966 |
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| Quelldatensatz | uspto-grants-1992_05 |
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| ORD ID | ord-ca7f59f82f7343c2823d7361a964354d |
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| Quellennotiz | uspto-grants-1992_05 |
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