HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium Hydroxide → Benzyl 4-(5-hydroxypyrazin-2-yl)phenylcarbamate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Chloropyrazine | HCID 73277 | — |
| Edukt | benzyl N-hydroxy-N-phenylcarbamate | HCID 12358018 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | Benzyl 4-(5-hydroxypyrazin-2-yl)phenylcarbamate | HCID 12358023 | — |
Reaktionsschritte
A solution of benzyl N-hydroxy-N-phenylcarbamate (8.0 g) in ethanolic potassium hydroxide (0.27N; 120 ml) was treated with chloropyrazine (4.18 g) and molecular sieve (0.5 g). The mixture was stirred for 2 hours at room temperature and then allowed to stand for 4 days. Evaporation of the reaction mixture under reduced pressure gave an orange residue which was suspended in dilute acetic acid, filtered off, and heated in hot 1-propanol (about 200 ml). On cooling, the resulting solution gave a golden precipitate of 5-(4-benzyloxycarbonylaminophenyl)-2(1H)-pyrazinone m.p. 240°-4° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04556711 |
| Quelldatensatz | uspto-grants-1985_12 |
| ORD ID | ord-617cfc8d7f31418f9f2dec206d122464 |
| Quellennotiz | uspto-grants-1985_12 |