Styrene Oxide → 2-Allylamino-1-phenyl-ethanol
反応式
[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]参加物
3
実験手順
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).
後処理
- temperaturewas heated
- temperatureto reflux under nitrogen atmosphere, for 24 hours
- temperatureUpon cooling
- customproduct crystallized
- customwas triturated with hexane
- customRecrystallization from hexane
出典と根拠
- ORDレコード
- ord-cc843f7929f04dc0a82af1ef5073e075
- 出典データセット
- uspto-grants-1989_11
- 特許番号
- US04882429
反応ノート
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