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

HRID 3932Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 3932
[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

Komponenten

5

Edukt 3

HCID 14798Sodium HydroxideHCID 1725484Phenol, 4-(5-octyl-2-pyridinyl)-HCID 14069923(R)-1-bromo-(4-methyl)decane

Produkt 1

HCID 14069925(R)2-[p-(4-methyldecyloxy)phenyl]-5-octylpyridineAusbeute 47,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-db779db8732644f49d9a577c43124856
Quelldatensatz
uspto-grants-1988_02
Patentnummer
US04723018

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