Sodium Hydroxide → (R)2-[p-(4-methyldecyloxy)phenyl]-5-octylpyridine
反応式
[OH-].[Na+].[OH:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][C:13]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[CH:12][N:11]=2)=[CH:6][CH:5]=1.Br[CH2:25][CH2:26][CH2:27][C@H:28]([CH3:35])[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34]>O>[CH3:35][C@H:28]([CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])[CH2:27][CH2:26][CH2:25][O:3][C:4]1[CH:5]=[CH:6][C:7]([C:10]2[CH:15]=[CH:14][C:13]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[CH:12][N:11]=2)=[CH:8][CH:9]=1参加物
実験手順
20 ml of a 30% aqueous solution of sodium hydroxide was added dropwise to a mixture of 2 g (0.007 mol) of 2-(p-hydroxyphenyl)-5-octylpyridine and 1.65 g (0.007 mol) of (R)-1-bromo-(4-methyl)decane with stirring. The resulting solution was heated to a temperature between about 90° and 100° C. for 3 hours. 150 ml of water was added to the reaction solution and the organic layer was extracted with chloroform. After washing the extract three times with water, chloroform was removed by distillation. The residue was chromatographed over 2.5×100 (cm) of silica gel and developed with hexane and benzene. The effluent was repeatedly recrystallized from a mixture of methanol and acetone to yield 1.44 g (0.0033 mol) of (R)2-[p-(4-methyldecyloxy)phenyl]-5-octylpyridine.
後処理
- temperatureThe resulting solution was heated to a temperature between about 90° and 100° C. for 3 hours
- extractionthe organic layer was extracted with chloroform
- washAfter washing the
- extractionextract three times with water, chloroform
- customwas removed by distillation
- customThe residue was chromatographed over 2.5×100 (cm) of silica gel
- customThe effluent was repeatedly recrystallized from a mixture of methanol and acetone
出典と根拠
- ORDレコード
- ord-db779db8732644f49d9a577c43124856
- 出典データセット
- uspto-grants-1988_02
- 特許番号
- US04723018
反応ノート
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