Ammonia → HCID 68124883, Verbindung
Reaktionsgleichung
[C:1]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][NH:9][C:10](=[O:22])[C:11]1[CH:16]=[CH:15][C:14]([O:17][C:18]([F:21])([F:20])[F:19])=[CH:13][CH:12]=1)#[N:2].N.NCCCCCCCN[C:33](=[O:45])[C:34]1[CH:39]=[CH:38][C:37](OC(F)(F)F)=[CH:36][CH:35]=1.Cl.[CH2:47]([OH:49])C>[Ni]>[CH3:47][O:49][CH:5]([CH2:6][CH2:7][CH2:8][NH:9][C:10](=[O:22])[C:11]1[CH:12]=[CH:13][C:14]([O:17][C:18]([F:21])([F:19])[F:20])=[CH:15][CH:16]=1)[CH2:4][CH2:3][CH2:1][NH:2][C:33](=[O:45])[C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1Komponenten
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture containing 12 g. of N-(6-cyanohexyl)-4-trifluoromethoxybenzamide in 100 ml. of ethanol, 8 g. of ammonia and 4 g. of Raney nickel was hydrogenated at approximately 30° C. for a period of 5 hours. The reaction mixture was filtered and the solvent and excess ammonia were removed by heating in vacuo. The residual material was dissolved in 150 ml. of isopropyl alcohol acidified with ethanolic hydrogen chloride and the solution was concentrated in vacuo to about 100 ml. The solution was cooled in an ice bath and the solid that separated was collected, washed with cold isopropyl alcohol and ether, and dried at 60° C. in vacuo to yield 9 g. of N-(7-aminoheptyl)-4-trifluoromethoxybenzamide as its hydrochloride, m.p. 178°-181° C.
Aufarbeitung
- additionA mixture containing 12 g
- filtrationThe reaction mixture was filtered
- customthe solvent and excess ammonia were removed
- temperatureby heating in vacuo
- dissolutionThe residual material was dissolved in 150 ml
- concentrationthe solution was concentrated in vacuo to about 100 ml
- temperatureThe solution was cooled in an ice bath
- customthe solid that separated
- customwas collected
- washwashed with cold isopropyl alcohol and ether
- customdried at 60° C. in vacuo
- customto yield 9 g
Quellen und Nachweise
- ORD-Eintrag
- ord-09b8cfa10e944a16a20dd737f0b5ca38
- Quelldatensatz
- uspto-grants-1977_02
- Patentnummer
- US04009208
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