HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → 3-[(6-Methoxy-4-chromanylidene)amino]-2-oxazolidinone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 6-methoxychroman-4-one | HCID 4612168 | — |
| Edukt | 3-amino-1,3-oxazolidin-2-id-4-one | HCID 178514269 | — |
| Katalysator | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 3-[(6-Methoxy-4-chromanylidene)amino]-2-oxazolidinone | HCID 70615282 | — |
Reaktionsschritte
A solution of 62 g (0.61 mole) of 3-amino-2-oxazolidone in 650 ml of benzene was treated with 15 drops of HCl (isopropanol) solution using mechanical stirring, and refluxed until all water was removed via a Dean-Stark trap. The solution was then treated with 107 g (0.60 mole) of 6-methoxy-4-chromanone and refluxed for 11.5 hr. A 9.6 ml portion of water (theory: 10.8 ml) was collected. The reaction mixture was stripped of benzene under the water pump. The residue was taken up in 200 ml of 1:1 isopropanol:ether, stored 24 hr at room temperature, refrigerated overnight and filtered. The resultant cream-colored solid was washed with 125 ml of isopropanol, ether, and dried. M.p. 54°-64°; yield: 115 g (73%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04093627 |
| Quelldatensatz | uspto-grants-1978_06 |
| ORD ID | ord-a2a0b1b410ce48e0bda49330495e0e76 |
| Quellennotiz | uspto-grants-1978_06 |