Sodium Hydroxide → (R)2-[p-(4-methyldecyloxy)phenyl]-5-octylpyridine

HRID 3932ノート

反応式

HRID 3932 の反応式
[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

5

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

  1. temperatureThe resulting solution was heated to a temperature between about 90° and 100° C. for 3 hours
  2. extractionthe organic layer was extracted with chloroform
  3. washAfter washing the
  4. extractionextract three times with water, chloroform
  5. customwas removed by distillation
  6. customThe residue was chromatographed over 2.5×100 (cm) of silica gel
  7. 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

読み込み中…