Reaktionsgleichung
[C:1]1([CH2:7][CH2:8][NH2:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:10](OCC)=[O:11]>>[CH2:8]([NH:9][CH:10]=[O:11])[CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Komponenten
3
Reaktionsbedingungen
- Temperatur
- 50 °C
Versuchsvorschrift
Into a 100-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 2-phenylethanamine (1.9 g, 15.70 mmol, 1.00 equiv). This was followed by the addition of ethyl formate (5 g, 67.57 mmol, 4.30 equiv) dropwise with stiffing. The resulting solution was stirred overnight at 50° C. The resulting solution was concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/methanol (70:1). This resulted in 2.27 g (97%) of N-phenethylformamide as yellow oil.
Aufarbeitung
- customInto a 100-mL 3-necked round-bottom flask purged
- temperaturemaintained with an inert atmosphere of nitrogen
- concentrationThe resulting solution was concentrated under vacuum
- customThis resulted in 2.27 g (97%) of N-phenethylformamide as yellow oil
Quellen und Nachweise
- ORD-Eintrag
- ord-3297cd83d6744d5c9fce381b2a37e689
- Quelldatensatz
- uspto-grants-2015_11
- Patentnummer
- US09193693B2
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