反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:20][O:21][C:22]([O:24][C:25]1[CH:30]=[CH:29][C:28]([C:31]2[CH:36]=[CH:35][C:34]([C:37]([OH:39])=[O:38])=[CH:33][CH:32]=2)=[CH:27][CH:26]=1)=[O:23].[CH2:40](O)[CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH3:47].N(C(OCC)=O)=NC(OCC)=O>O1CCCC1>[CH2:40]([O:38][C:37]([C:34]1[CH:35]=[CH:36][C:31]([C:28]2[CH:27]=[CH:26][C:25]([O:24][C:22]([O:21][CH3:20])=[O:23])=[CH:30][CH:29]=2)=[CH:32][CH:33]=1)=[O:39])[CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH3:47]参加物
実験手順
A solution of triphenylphosphine (3.78 g, 0.014 mol) in dry tetrahydrofuran (50 ml) was added to a stirred solution of compound 4 (3.92 g, 0.014 mol), octan-1-ol (1.88 g, 0.014 mol) and diethyl azodicarboxylate (DEAD) (2.51 g, 0.014 mol) in dry tetrahydrofuran (100 ml) under an atmosphere of dry nitrogen. The addition was such that the triphenylphosphine was added over 30 seconds in which time the solution became hot and the white solid (4) and orange colour (DEAD) disappeared. The resultant solution was stirred overnight, the solvent was removed in vacuo and the viscous, oily residue was purified by column chromatography (10% petrol/dichloromethane) to give a colourless solid which was recrystallised from ethanol to leave colourless plates.
後処理
- additionThe addition
- additionwas added over 30 seconds in which time the solution
- customthe solvent was removed in vacuo
- customthe viscous, oily residue was purified by column chromatography (10% petrol/dichloromethane)
- customto give a colourless solid which
- customwas recrystallised from ethanol
- customto leave colourless plates
出典と根拠
- ORDレコード
- ord-84ebbcc068df4f88a51e1edae094ac0a
- 出典データセット
- uspto-grants-1999_04
- 特許番号
- US05891358
関連ノート
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