HCID 68147811, Verbindung → HCID 21553917, Verbindung
Reaktionsgleichung
[CH:1]([N:4]1[CH2:8][C:7]2([CH2:14][O:13][C:12]3[CH:15]=[CH:16][C:17]([NH:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])=[CH:18][C:11]=3[O:10][CH2:9]2)[O:6]C1=O)([CH3:3])[CH3:2]>C(O)C>[OH:6][C:7]1([CH2:8][NH:4][CH:1]([CH3:2])[CH3:3])[CH2:14][O:13][C:12]2[CH:15]=[CH:16][C:17]([NH:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])=[CH:18][C:11]=2[O:10][CH2:9]1Komponenten
3
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
This oxazolidinone from Step A above is refluxed in ethanol containing anhydrous hydrogen chloride. The solution is neutralized, evaporated to a small volume, diluted with water and extracted with ether. The dried etheral solution is evaporated to give the desired product.
Aufarbeitung
- customevaporated to a small volume
- additiondiluted with water
- extractionextracted with ether
- customThe dried etheral solution is evaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-c6776d48462e4869873a3c58f3c6686b
- Quelldatensatz
- uspto-grants-1976_03
- Patentnummer
- US03944560
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