Water → Ethyl 4-({3-[4-(benzyloxy)phenyl]propyl}amino)benzoate
Reaktionsgleichung
CS(O[CH2:6][CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:11][CH:10]=1)(=O)=O.CN(C)P(N(C)C)(N(C)C)=O.[NH2:34][C:35]1[CH:45]=[CH:44][C:38]([C:39]([O:41][CH2:42][CH3:43])=[O:40])=[CH:37][CH:36]=1.O>C(O)C>[CH2:16]([O:15][C:12]1[CH:13]=[CH:14][C:9]([CH2:8][CH2:7][CH2:6][NH:34][C:35]2[CH:36]=[CH:37][C:38]([C:39]([O:41][CH2:42][CH3:43])=[O:40])=[CH:44][CH:45]=2)=[CH:10][CH:11]=1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 12.8 g. of 3-[p-(benzyloxy)phenyl]propanol O-methanesulfonate (prepared as described in Example 43), 50 ml. of hexamethylphosphoramide and 16.5 g. of ethyl p-aminobenzoate is heated at 100°-105° C. for 17.5 hours. The mixture is chilled, diluted with 15 ml. of water, 30 ml. of ethanol and chilled. In order to filter, 100 ml. of ethanol-water (1:1) is added and the solid filtered and washed with ethanol-water (1:1) and with water to give tan crystals, m.p. 98°-107° C. Recrystallization from ethanol gives light tan crystals, m.p. 114°-116° C.
Aufarbeitung
- additionA mixture of 12.8 g
- temperatureThe mixture is chilled
- additiondiluted with 15 ml
- filtrationIn order to filter
- additionof ethanol-water (1:1) is added
- filtrationthe solid filtered
- washwashed with ethanol-water (1:1) and with water
- customto give tan crystals, m.p. 98°-107° C
- customRecrystallization from ethanol
- customgives light tan crystals, m.p. 114°-116° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-d23ae89ae02b4af8a67acc297f0cb53b
- Quelldatensatz
- uspto-grants-1980_01
- Patentnummer
- US04185115
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