Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | Methyl 2-(3-methoxyphenoxy)phenylacetate | HCID 14620154 | — |
| Lösungsmittel | Dimethyl Carbonate | HCID 12021 | — |
| Produkt | HCID 54488544 | HCID 54488544 | — |
Reaktionsschritte
Methyl 2-(3-methoxyphenoxy)phenylacetate (6.81 g) was dissolved in 11 mL of dimethyl carbonate and 600 mg of sodium was added. The mixture was heated at reflux for 10 h, then cooled. The reaction mixture was quenched with water, acidified with concentrated aqueous HCl and extracted with dichloromethane. The combined organic extracts were dried (MgSO4), filtered and concentrated under reduced pressure to give an oil. The desired material was separated from unreacted starting material by flash chromatography (4:1 hexane: ethyl acetate as eluant) to yield after concentration, 3.54 g (43%) of the title compound of Step B. 1H NMR (CDCl3): δ7.46(dd,J=1.5,7.5Hz,1H), 7.29 (t,J=8Hz,1H), 7.2 (m,2H), 6.92 (d,J=8Hz,1H), 6.65 (td, J=1.5,7.5Hz,1H), 6.5 (m,2H), 5.14 (s,1H), 3.77 (s,3H), 3.73 (s,6H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05747516 |
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| Quelldatensatz | uspto-grants-1998_05 |
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| ORD ID | ord-dffc1669862a402dbdc6dbd3f939f6b9 |
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| Quellennotiz | uspto-grants-1998_05 |
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