Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Methyl Acrylate | HCID 7294 | — |
| Edukt | P-Anisidine | HCID 7732 | — |
| Edukt | Pentyl nitrite | HCID 10026 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-Methoxycinnamate methyl ester | HCID 92841 | 87% |
Reaktionsschritte
117 g of amyl nitrite are added slowly to a solution, cooled to about 10° C., of 123 g of p-anisidine and 100 ml of conc. H2SO4 in 400 ml of methanol and the mixture is stirred without cooling for a further 40 minutes after addition is complete It is treated with 95 g of methyl acrylate and 112 mg of Pd(OAc)2 and heated to about 55° C. until evolution of gas has ended. After cooling, the solid is filtered off with suction, washed with water and dried at 40° C. 167 g (87%) of methyl p-methoxycinnamate are obtained, m.p. 88°-89° C., Lit 89° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05231223 |
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| Quelldatensatz | uspto-grants-1993_07 |
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| ORD ID | ord-01bac67072f147ca90be166e658fb667 |
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| Quellennotiz | uspto-grants-1993_07 |
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