反応式
[OH:1][CH2:2][CH2:3][N:4]1[CH2:8][CH2:7][N:6]=[C:5]1[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16]/[CH:17]=[CH:18]\[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26].[C:27]([OH:46])(=[O:45])[CH2:28][CH2:29]CCCCC/C=C\CCCCCCCC.N[CH2:48][CH2:49]C(CN)O>>[OH:1][CH2:2][CH2:3][N:4]1[CH2:8][CH2:7][N:6]=[C:5]1[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16]/[CH:17]=[CH:18]\[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH:28]([C:27]([O:46][CH2:48][CH3:49])=[O:45])[CH3:29]参加物
4
実験手順
This example was carried out in the same manner as that in Example 1, except that 69.7 g (0.2 mol) of 1-(2-hydroxyethyl)-2-oleyl-2-imidazoline synthesized from oleic acid (AV 200, average molecular weight 280.5) and aminoethylethanolamine was used. 1-(2-hydroxyethyl)-2-(α-ethoxycarbonylethyl-oleyl)-2-imidazoline was obtained (yield 93.8%).
出典と根拠
- ORDレコード
- ord-ba22b1083d074e748acd83da16a25c36
- 出典データセット
- uspto-grants-1984_02
- 特許番号
- US04431672
関連ノート
読み込み中…