Styrene Oxide → 2-Allylamino-1-phenyl-ethanol
Reaktionsgleichung
[CH2:1]1[O:9][CH:2]1[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:10]([NH2:13])[CH:11]=[CH2:12]>>[CH2:10]([NH:13][CH2:1][CH:2]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1)[OH:9])[CH:11]=[CH2:12]Komponenten
3
Versuchsvorschrift
A mixture of styrene oxide (24 mL, 0.2 moles) and allylamine (60.8 mL, 0.8 moles) was heated to reflux under nitrogen atmosphere, for 24 hours. Upon cooling, product crystallized and was triturated with hexane. Recrystallization from hexane afforded the title compound essentially uncontaminated by the other possible regioisomer. Ms m+/z=177; H1NMR (CDCl3): δ 7.3 (br.s, 5H), 5.6-6.1 (m, 1H), 4.9-5.4 (m, 2H), 4.75 (m, 1H), 3.2 (br.d, 2H), 2.9 (br.s, 2H), 2.7 (m, 2H).
Aufarbeitung
- temperaturewas heated
- temperatureto reflux under nitrogen atmosphere, for 24 hours
- temperatureUpon cooling
- customproduct crystallized
- customwas triturated with hexane
- customRecrystallization from hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-cc843f7929f04dc0a82af1ef5073e075
- Quelldatensatz
- uspto-grants-1989_11
- Patentnummer
- US04882429
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