HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 222322Erstellt: 25. Oktober 2026
1-(Diphenylmethyl)azetidin-3-one → 1-Benzhydryl-3-methylazetidin-3-ol
https://huagongshe.com/reaction/222322
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-(Diphenylmethyl)azetidin-3-one | HCID 3735558 | — |
| Edukt | HCID 178418373 | HCID 178418373 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1-Benzhydryl-3-methylazetidin-3-ol | HCID 10243989 | — |
Reaktionsschritte
Methyl magnesium iodide (3M in diethyl ether, 1.4 mL, 4.2 mmol) was added dropwise to an ice-cold solution of 1-(diphenylmethyl)-3-azetidinone (1 g, 4.20 mmol) in diethyl ether (25 mL) and the mixture was stirred for 1 hour at 0° C. The crude reaction mixture was then purified directly by column chromatography on silica gel, eluting with dichloromethane:methanol, 100:0 to 95:5, to afford the title compound the title compound as a pale yellow oil in 68% yield, 730 mg. 1H NMR (CDCl3, 400 MHz) δ: 1.54 (s, 3H), 3.02 (m, 2H), 3.22 (m, 2H), 4.39 (s, 1H), 7.20 (m, 4H), 7.26 (m, 4H), 7.41 (m, 2H); LRMS ESI+ m/z 254 [M+H]+
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08207198B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-35d7b925ab3e4019baa5591dbc185372 |
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| Quellennotiz | uspto-grants-2012_06 |
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