Ethanol → 5-Benzyl-3-(chloromethyl)-1,2,4-oxadiazole
反応式
[Cl:1][CH2:2][C:3](=[N:5][OH:6])[NH2:4].Cl.[C:8]1(N=CC(OCC)=O)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH2:21](O)[CH3:22]>>[Cl:1][CH2:2][C:3]1[N:4]=[C:21]([CH2:22][C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[O:6][N:5]=1参加物
4
実験手順
A mixture of chloroacetamide oxime, 11.0 g. (0.10 mole), and ethyl phenyliminoacetate hydrochloride, 22 g. (0.11 mole), in 80 ml. of absolute ethanol is refluxed for one hour. After cooling, the ammonium chloride which precipitates is filtered off and the alcohol is removed in vacuo. Upon steam distillation of the residue, 7.0 gm. of 3-chloromethyl-5-benzyl-1,2,4-oxadiazole is obtained, n20 1.5386.
後処理
- temperatureAfter cooling
- customthe ammonium chloride which precipitates
- filtrationis filtered off
- customthe alcohol is removed in vacuo
- distillationUpon steam distillation of the residue, 7.0 gm
出典と根拠
- ORDレコード
- ord-c563bab3674c40f2bb308f1a8f37b253
- 出典データセット
- uspto-grants-1976_05
- 特許番号
- US03956498
反応ノート
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