Sulfuric Acid → 4-(Methylsulfonyl)phenol

HRID 2070231Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2070231
C1[C:6]([C@H:7]([CH2:12][NH2:13])[CH2:8][C:9]([OH:11])=[O:10])=[CH:5][CH:4]=C(Cl)C=1.[C:15](=[O:18])([O-:17])[O-].[K+].[K+].[CH3:21][CH:22]([CH3:44])[C:23]([O:25][CH:26](OC([O:33][C:34]1[CH:39]=[CH:38][C:37]([S:40]([CH3:43])(=[O:42])=[O:41])=[CH:36][CH:35]=1)=O)[CH:27](C)C)=[O:24].S(=O)(=O)(O)O.[C:50](#N)C>COC(C)(C)C.O>[CH3:50][CH:5]([CH3:4])[CH2:6][C@H:7]([CH2:12][NH:13][C:15]([O:17][CH2:27][CH2:26][O:25][C:23](=[O:24])[CH:22]([CH3:44])[CH3:21])=[O:18])[CH2:8][C:9]([OH:11])=[O:10].[CH3:43][S:40]([C:37]1[CH:38]=[CH:39][C:34]([OH:33])=[CH:35][CH:36]=1)(=[O:41])=[O:42]

Komponenten

9

Versuchsvorschrift

R-Baclofen (2.13 g) and water (50 mL) were charged to a vessel at room temperature. Potassium carbonate (1.6 g) was added in one portion and the mixture was stirred at room temperature for 5 minutes. A solution of 2-methyl-1-[4-(methylsulfonyl)phenoxycarbonyloxy]propyl 2-methylpropanoate D6 (3.5 g) in acetonitrile (50 mL) was added. After 6 hours, tert-butyl methyl ether (50 mL) was added and the reaction mixture was cooled to 5-10° C. A 5% aqueous sulfuric acid was added to adjust the pH to approximately 3. The mixture was then warmed to room temperature and stirred for 10 minutes. The organic layer was washed with water (3×20 mL) and evaporated to provide the crude title compound as an orange oil with 4-(methylsulfonyl)phenol impurity.

Aufarbeitung

  1. waitAfter 6 hours
  2. temperaturethe reaction mixture was cooled to 5-10° C
  3. temperatureThe mixture was then warmed to room temperature
  4. stirringstirred for 10 minutes
  5. washThe organic layer was washed with water (3×20 mL)
  6. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-037d556ae9d74d86ab682802c1ce4935
Quelldatensatz
uspto-grants-2012_10
Patentnummer
US08299291B2

Notizen zur Reaktion

Wird geladen…