Ammonium Chloride → 2-Cyclohexyl-2-hydroxy-2-thien-2-ylacetic Acid Methyl Ester

HRID 1360617Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1360617
[CH:1]1([Mg]Cl)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:9][O:10][C:11](=[O:19])[C:12](=[O:18])[C:13]1[S:14][CH:15]=[CH:16][CH:17]=1.[Cl-].[NH4+]>C(OCC)C.C1COCC1>[CH3:9][O:10][C:11](=[O:19])[C:12]([CH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1)([OH:18])[C:13]1[S:14][CH:15]=[CH:16][CH:17]=1

Komponenten

6

Edukt 3

HCID 25517Ammonium ChlorideHCID 11217486Methyl alpha-oxo-2-thiopheneacetateHCID 178478990HCID 178478990, Verbindung

Produkt 1

HCID 669594652-Cyclohexyl-2-hydroxy-2-thien-2-ylacetic Acid Methyl Ester

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283Diethyl EtherLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

98.6 ml (0.197 mol) of a 2M solution of Cyclohexylmagnesium chloride in diethyl ether, were added to a solution of 27.97 g (0.164 mol) of 2-oxo-2-thien-2-ylacetic acid methyl ester dissolved in 370 ml of THF, at −78° C. under a N2 atmosphere. The mixture was stirred at this temperature for 10 minutes, and then warmed to room temperature. After 1 h, the reaction mixture was treated with a saturated solution of ammonium chloride and extracted three times with ethyl acetate. The organic phases were combined, washed with water, and dried over MgSO4. After removal of the solvent, the oil obtained was purified by column chromatography (silica gel) using hexane/AcOEt 90:10 as eluent. The yield was 16.2 g (39.5%) of a pure product, whose structure was confirmed by 1H-NMR.

Aufarbeitung

  1. waitAfter 1 h
  2. extractionextracted three times with ethyl acetate
  3. washwashed with water
  4. dry with materialdried over MgSO4
  5. customAfter removal of the solvent
  6. customthe oil obtained
  7. customwas purified by column chromatography (silica gel)

Quellen und Nachweise

ORD-Eintrag
ord-b3ec87953ec14c91b2ccbce5f45b2130
Quelldatensatz
uspto-grants-2011_02
Patentnummer
US07879874B2

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