HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-(4-Aminophenyl)-4-oxobutanoic acid → 3-[p-(1-Chlorocyclopropylcarbonylamino)-benzoyl]-propionic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-(4-Aminophenyl)-4-oxobutanoic acid | HCID 243290 | — |
| Edukt | Cyclopropanecarbonyl chloride, 1-chloro- | HCID 10942508 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-[p-(1-Chlorocyclopropylcarbonylamino)-benzoyl]-propionic acid | HCID 20483371 | 49,3% |
Reaktionsschritte
3.9 g (28.1 millimoles) of 1-chlorocyclopropanecarboxylic acid chloride are added, with stirring, to 4.5 g (23.3 millimoles) of 3-(p-aminobenzoyl)-propionic acid in 100 ml of absolute tetrahydrofuran. The reaction mixture is then stirred for 20 hours at room temperature, followed by 7 hours under reflux. A small amount of solid is filtered off and discarded, and the filtrate is concentrated. The residue obtained is recrystallized from ethyl acetate, giving 3.4 g (49% of theory) of 3-[p-(1-chlorocyclopropylcarbonylamino)-benzoyl]-propionic acid as colorless crystals, of melting point 178°-179° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04410529 |
| Quelldatensatz | uspto-grants-1983_10 |
| ORD ID | ord-74d38cc0253c41d886bfa8b64df79659 |
| Quellennotiz | uspto-grants-1983_10 |