HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Phthalaldehydic acid → 5-(4-(1-Oxoisoindoline-2-yl)Phenyl)Thiazolidine-2,4-Dione
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Phthalaldehydic acid | HCID 8406 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 5-(4-Aminophenyl)thiazolidine-2,4-dione | HCID 12850972 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 5-(4-(1-Oxoisoindoline-2-yl)Phenyl)Thiazolidine-2,4-Dione | HCID 19086265 | 90,4% |
Reaktionsschritte
Into 50 ml of ethanol were dissolved 4.90 g of 5-(4-aminophenyl)-thiazolidine-2,4-dione and 3.54 g of phthalaldehydic acid, and the solution was refluxed for 2 hours. After cooling by standing, 1.78 g of sodium borohydride were added and the mixture was stirred for 20 minutes at room temperature. Thereafter, solvent was distilled off under reduced pressure and 10 ml of glacial acetic acid were added to the residue, which was stirred for 10 minutes at 100 ° C. After cooling by standing, 100 ml of water were added and the crystals deposited were collected by filtration, washed with water and dried. These were recrystallized from ethanol to obtain 6.90 g of title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05308856 |
| Quelldatensatz | uspto-grants-1994_05 |
| ORD ID | ord-720e7ed39ba74a2ea9b99e00f6037b11 |
| Quellennotiz | uspto-grants-1994_05 |