Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-(2-Methoxyphenoxy)acetic acid | HCID 15882 | — |
| Edukt | Metampicillin | HCID 6713928 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Talampicillin 2-methoxyphenoxyacetate | HCID 86738030 | — |
Reaktionsschritte
To a solution of 20.4 g of phthalidyl ester of metampicillin in 100 ml of ethyl acetate there is added a solution of 40 ml of N hydrochloric acid in 120 ml of water. The mixture is maintained under stirring for 45 minutes at room temperature, the organic phase is separated off and the aqueous phase is washed twice with diethyl ether. The aqueous solution is let stand for 20 minutes at 20° C. under reduced pressure, and then it is filtered through asbestos pretreated with hydrochloric acid. To the clear solution thus obtained, there is added, quickly, drop by drop and under stirring a solution of 8 g of 2-methoxyphenoxyacetic acid in 100 ml of water containing 1.76 g of sodium hydroxide. The precipitate which forms is filtered, washed with water and dried on P2O5 at room temperature and under reduced pressure, to give the talampicillin 2-methoxyphenoxyacetate; m.p. 105°-110° C. (dec.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04293560 |
|---|
| Quelldatensatz | uspto-grants-1981_10 |
|---|
| ORD ID | ord-51b9a76471df4af79a23646e125583db |
|---|
| Quellennotiz | uspto-grants-1981_10 |
|---|