Ethyl formate → N-[2-(4-Bromophenethyl)-phenethyl]-formamide
Reaktionsgleichung
[Br:1][C:2]1[CH:18]=[CH:17][C:5]([CH2:6][CH2:7][C:8]2[CH:16]=[CH:15][CH:14]=[CH:13][C:9]=2[CH2:10][CH2:11][NH2:12])=[CH:4][CH:3]=1.[CH:19](OCC)=[O:20]>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][CH2:7][C:8]2[CH:16]=[CH:15][CH:14]=[CH:13][C:9]=2[CH2:10][CH2:11][NH:12][CH:19]=[O:20])=[CH:17][CH:18]=1Komponenten
3
Versuchsvorschrift
A solution of 0.60 g. (0.00197 mole) of 2-(4-bromophenethyl)-phenethylamine in 20 ml. of ethyl formate is heated to refluxing for about 19 hours. The solution is evaporated to dryness under reduced pressure and the residue dissolved in dry benzene. Evaporation of the solvent under reduced pressure leaves the product as the residual yellow oil.
Aufarbeitung
- temperatureto refluxing for about 19 hours
- customThe solution is evaporated to dryness under reduced pressure
- dissolutionthe residue dissolved in dry benzene
- customEvaporation of the solvent under reduced pressure
- customleaves the product as the residual yellow oil
Quellen und Nachweise
- ORD-Eintrag
- ord-ccdf027adc2643048b1178f27d10e492
- Quelldatensatz
- uspto-grants-1976_10
- Patentnummer
- US03988454
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