HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetic Acid → Methyl 5-methylamino-3-hydroxy-2-methyl-3-indenylacetate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Methyl 3-hydroxy-2-methyl-5-nitro-3-indenylacetate | HCID 53908697 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Methyl 5-methylamino-3-hydroxy-2-methyl-3-indenylacetate | HCID 53799079 | — |
Reaktionsschritte
A solution of 0.05 mol of methyl 3-hydroxy-2-methyl-5-nitro-3-indenylacetate, 0.2 mol of 38% aqueous formaldehyde and 2 ml of acetic acid in 100 ml ethanol is reduced catalytically in the presence of a 10% Pd/C catalyst under 40 lb. p.s.i. hydrogen pressure at room temperature. The solution is filtered, evaporated and chromatographed on 300 g of silica gel to give methyl 5-methylamino-3-hydroxy-2-methyl-3-indenylacetate. The hydroxy ester is then dehydrated to methyl 5-dimethylamino-2-methyl-3-indenylacetate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05696159 |
| Quelldatensatz | uspto-grants-1997_12 |
| ORD ID | ord-b228eb8260bc470abbc6b42494622822 |
| Quellennotiz | uspto-grants-1997_12 |