HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1099016Erstellt: 25. Oktober 2026
m-Chloroperbenzoic acid → Methyl 2-phenyloxirane-2-carboxylate
https://huagongshe.com/reaction/1099016
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Edukt | Methyl atropate | HCID 193334 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Methyl 2-phenyloxirane-2-carboxylate | HCID 12594817 | — |
Reaktionsschritte
The title compound was synthesized according to a literature method (Whitman Tetrahedron 1985, 41, 1183). To a mixture of 2-phenylacrylic acid methyl ester (7.92 g, 45 mmol) in 60 ml of methylene chloride was added mCPBA (13.1 g, 58.5 mmol) and the reaction was stirred at 45° C. overnight. The reaction mixture was then filtered and the solid was washed with methylene chloride. The filtrate was washed three times with 50 ml of equal parts solution consisting of saturated Na2S2O3 and saturated NaHCO3. The organic layer was washed with water and brine, dried over MgSO4, and concentrated under reduced pressure to afford the title compound in greater than 95% purity according to 1H NMR (85% yield). 1H NMR (CDCl3, 300 MHz) δ: 7.50-7.30 (m, 5H), 4.22 (q, J=7.2 Hz, 2H), 3.40 (d, J,=7.1 Hz, 1H), 2.95 (d, J=7.1 Hz, 1H), 1.26 (t, J=7.2 Hz, 3H) ppm.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08143375B2 |
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| Quelldatensatz | uspto-grants-2012_03 |
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| ORD ID | ord-46764ac44eeb423e97af8d2be89458ee |
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| Quellennotiz | uspto-grants-2012_03 |
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