Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Dimethyl Sulfate | HCID 6497 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Methyl 2-(2'-benzyloxyphenyl)-3-hydroxyacrylate | HCID 69942437 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Methyl 2-(2-(benzyloxy)phenyl)-3-methoxyacrylate | HCID 838698 | — |
| Produkt | Methyl 2-(2-(benzyloxy)phenyl)acetate | HCID 11076055 | — |
Reaktionsschritte
The crude methyl 3-hydroxy-2-(2'-benzyloxyphenyl)propenoate was dissolved in dry DMF (100 ml) and potassium carbonate (29.0 g) was added in one portion. Dimethyl sulphate (16.00 g) in dry DMF (10 ml) was then added dropwise with stirring. After ninety minutes, water (300 ml) was added and the solution was extracted with ether (2 x 300 ml). After washing with water (3 x 150 ml) and brine, the extracts were dried and concentrated under reduced pressure, and the resulting yellow oil solidified on trituration with ether/petrol. Recrystallization from dry methanol afforded E-methyl 3-methoxy-2-(2'-benzyloxyphenyl)propenoate as a white, crystalline solid (5.44g, 17% yield from methyl 2-benzyloxyphenylacetate), M.P. 76-77° C.; infrared maxima (nujol mull): 1710, 1640 cm-1 ; 1H nmr (CDCl3, 90MHz): delta 3.63 (3H,s), 3.75 (3H,s), 5.05 (2H,s), 6.80-7.40 (9H,m), 7.50 (1H,s)ppm.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05034388 |
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| Quelldatensatz | uspto-grants-1991_07 |
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| ORD ID | ord-a1c0d762440c4a9c8b15d14b0891577c |
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| Quellennotiz | uspto-grants-1991_07 |
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