Sodium Hydroxide → Phenol

HRID 611204Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 611204
Cl.[O:2]1[C:6]2[CH2:7][NH:8][CH2:9][CH2:10][C:5]=2[CH:4]=[CH:3]1.[OH-].[Na+].O1C2CNCCC=2C=C1.[C:22](=O)([O:30][CH2:31][CH2:32][CH2:33][CH2:34][C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1)[O:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>O.N1C=CC=CC=1>[C:35]1([CH2:34][CH2:33][CH2:32][CH2:31][O:30][C:22]([N:8]2[CH2:9][CH2:10][C:5]3[CH:4]=[CH:3][O:2][C:6]=3[CH2:7]2)=[O:23])[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1.[C:24]1([OH:23])[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

Komponenten

8

Versuchsvorschrift

4,5,6,7-Tetrahydrofuro[2,3-c]pyridine hydrochloride 0.280 g (1.754 mmol) was dissolved in water. The solution was alkalified with aqueous sodium hydroxide and extracted with dichloromethane 3 times. The combined organic layer was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. A solution of the resulting crude 4,5,6,7-tetrahydrofuro[2,3-c]pyridine and 0.71 g (2.6 mmol) of phenyl 4-phenylbutyl carbonate in 10 ml of pyridine was stirred at 100° C. overnight. The solvent was distilled off under reduced pressure; the resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate=15/1 to 9/1) to yield 6-(4-phenylbutoxycarbonyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridine as a mixture with phenol.

Aufarbeitung

  1. extractionextracted with dichloromethane 3 times
  2. dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
  3. distillationthe solvent was distilled off under reduced pressure
  4. distillationThe solvent was distilled off under reduced pressure
  5. customthe resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate=15/1 to 9/1)

Quellen und Nachweise

ORD-Eintrag
ord-359843f0692a49a182fc3bbf482bea6d
Quelldatensatz
uspto-grants-1999_12
Patentnummer
US05998433

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