Réaction #87169

ord-5683a11f2fe443e6839b40159d080476

Équation de réaction

[Cl-].[NH4+]
NH4Cl
[Li][CH3]
MeLi
CCOC(=O)C1CCC(=O)CC1
ethyl 4-oxocyclohexanecarboxylate
CCOC(=O)C1CCC(C)(O)CC1
ethyl 4-hydroxy-4-methylcyclohexanecarboxylate
Rendement 41.0%

Conditions de réaction

Température
-60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionthe resulting mixture was extracted with EtOAc (100 mL×2)
  2. 2
    LavageThe combined organic layers were washed with brine (150 mL) and water (150 mL)
  3. 3
    Séchagedried over anhydrous sodium sulfate
  4. 4
    Concentrationconcentrated
  5. 5
    AutreThe residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=10:1)

Mode opératoire

To a solution of ethyl 4-oxocyclohexanecarboxylate (4.00 g, 23.5 mmol) in diethyl ether (80 mL) was added MeLi (37.6 mL, 1M in diethyl ether) at −60° C. under nitrogen atmosphere. The reaction mixture was stirred at −60° C. for 30 min. Saturated aqueous NH4Cl (50 mL) was added and the resulting mixture was extracted with EtOAc (100 mL×2). The combined organic layers were washed with brine (150 mL) and water (150 mL), dried over anhydrous sodium sulfate, and concentrated. The residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=10:1) to afford ethyl 4-hydroxy-4-methylcyclohexanecarboxylate (1.8 g, 41% yield) as an oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09434761B2uspto-grants-2016_09