HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3,5-Dinitrobenzoyl chloride → 3-(3,5-Dinitrobenzoyl)-1,3-thiazolidine-2-thione
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3,5-Dinitrobenzoyl chloride | HCID 7432 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Thiazolidinethione | HCID 2723699 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-(3,5-Dinitrobenzoyl)-1,3-thiazolidine-2-thione | HCID 13217634 | 70,6% |
Reaktionsschritte
To 15 ml of dimethylformamide were dissolved 3,5-dinitrobenzoyl chloride (2.5 g) and 1,3-thiazolidine-2-thione (1.3 g). To the solution was added dropwise a solution of triethyl amine (1.2 g) and dimethylformamide (2 ml) under ice-cooling. The mixture was stirred under ice-cooling for 1 hour and at room temperature for 5 hours. The reaction mixture was filtered and the solvent was removed at a reduced pressure. To the residue was added water and the insolubles were filtered off. The filtrate was washed with cold methanol and then with ether to obtain crude crystals. Recrystallization from toluene gives 2.4 g of the desired compound as yellow needle crystals (yield 76.7%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04474814 |
| Quelldatensatz | uspto-grants-1984_10 |
| ORD ID | ord-703010360b4043f88bac8de847b9c85d |
| Quellennotiz | uspto-grants-1984_10 |