Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Allylbenzene | HCID 9309 | — |
| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-(Phenylmethyl)oxirane | HCID 94826 | 77% |
Reaktionsschritte
A solution of m-chloroperbenzoic acid (mCPBA; 17 g, 0.1 mol) in 120 mL of methylene chloride was added (at ambient temperature) dropwise to a solution of allyl benzene (10 g, 85 mmol) in 200 mL of methylene chloride. After the reaction mixture was stirred for 5 h with a mechanical stirrer, 5 additional grams of m-CPBA were added and the reaction mixture stirred for another 2 h. The reaction mixture was then diluted with 200 mL of ether, washed with 2×100 mL of aqueous sodium bisulfite solution, 1×100 mL of aqueous sodium bicarbonate solution and 1×100 mL of brine. The organic solution was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by bulb-to-bulb distillation (60° C., 0.1 mm) to give 8.5 g (77% yield) of 1-benzyl ethylene oxide as a clear colorless liquid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05591884 |
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| Quelldatensatz | uspto-grants-1997_01 |
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| ORD ID | ord-5d0c3ceb88b24351855dd081b6f954a1 |
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| Quellennotiz | uspto-grants-1997_01 |
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