反応式
[CH2:1]([N:17]=[C:18]=[S:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[CH2:20]=[C:21]([CH2:24][OH:25])[CH2:22][OH:23]>CN(C)C1C=CN=CC=1.N1C=CC=CC=1>[CH2:1]([NH:17][C:18]([O:23][CH2:22][C:21](=[CH2:20])[CH2:24][OH:25])=[S:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]参加物
5
実験手順
Hexadecyl isothiocyanate (9.65 g) and 2-methylenepropane-1,3-diol) (3.0 g) were heated with pyridine (17 ml) and 4-dimethylaminopyridine (0.8 g) to 104° C. for 6.5 hours. The mixture was evaporated to dryness in vacuo and chromatographed on a Waters PrepLC®/System 500A using a PrepPAK®-500/SILICA cartridge with ether/chloroform/hexane 2:2:9 as eluent.
後処理
- customThe mixture was evaporated to dryness in vacuo
- customchromatographed on a Waters PrepLC®/System 500A
出典と根拠
- ORDレコード
- ord-818d377f8cbf4779a998dd70ca11179a
- 出典データセット
- uspto-grants-1990_07
- 特許番号
- US04945098
関連ノート
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