Hydrochloric Acid → HCID 69462263, Verbindung
Reaktionsgleichung
Cl[C:2](OC1C=CC=CC=1)=[O:3].[NH2:11][C:12]1[C:13]([OH:29])=[C:14]([C:26](=[O:28])[CH3:27])[CH:15]=[CH:16][C:17]=1[O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.Cl>N1C=CC=CC=1>[C:26]([C:14]1[C:13]2[O:29][C:2](=[O:3])[NH:11][C:12]=2[C:17]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[CH:16][CH:15]=1)(=[O:28])[CH3:27]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 92.5 °C
Versuchsvorschrift
41 mL phenyl chloroformate are added dropwise to a solution of 47 g (183 mmol) 1-(3-amino-4-benzyloxy-2-hydroxy-phenyl)-ethanone (known from U.S. Pat. No. 4,460,581) in 135 mL pyridine, whereupon the temperature rises to 75° C. The mixture is stirred for 4 hours at 90-95° C., poured onto ice and acidified with hydrochloric acid. The precipitated solid is suction filtered, washed with diethyl ether and heated in 500 mL 95% acetonitrile for 30 minutes at reflux temperature. After cooling the solid is filtered off and washed with acetonitrile and diethyl ether.
Aufarbeitung
- customrises to 75° C
- additionpoured onto ice
- filtrationfiltered
- washwashed with diethyl ether
- temperatureheated in 500 mL 95% acetonitrile for 30 minutes
- temperatureat reflux temperature
- temperatureAfter cooling the solid
- filtrationis filtered off
- washwashed with acetonitrile and diethyl ether
Quellen und Nachweise
- ORD-Eintrag
- ord-5a694cac4c154f0a9f5479c0a7f8ca4c
- Quelldatensatz
- uspto-grants-2007_12
- Patentnummer
- US07307076B2
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