Reaktion #48651

ord-d627f1bf619d45f9a308e90a73367594

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeQuench with 10% aqueous potassium carbonate (10 mL)
  2. 2
    Extraktionextract with ethyl acetate (3×50 mL)
  3. 3
    WaschenCombine the organic extracts, wash with 0.1 N aqueous citric acid (30 mL) and 1 N lithium chloride
  4. 4
    Trocknendry (magnesium sulfate)
  5. 5
    Einengenconcentrate
  6. 6
    Sonstigecrystallize with xylenes

Vorschrift

Add 1-hydroxybenzotriazole (HOBT) (1.46 g, 10.8118 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDCI) (2.07 g, 10.8118 mmol) to a solution of crude trans-cyclopropane-1,2-dicarboxylic acid monoethyl ester (1.71 g, 10.8118 mmol) in N,N-dimethylformamide (11 mL). Stir for 30 minutes. Add triethylamine (2.26 mL, 16.2177 mmol) and methylpropylamine (1.11 mL, 10.8118 mmol) and stir for 16 hours. Quench with 10% aqueous potassium carbonate (10 mL) and extract with ethyl acetate (3×50 mL). Combine the organic extracts, wash with 0.1 N aqueous citric acid (30 mL) and 1 N lithium chloride, dry (magnesium sulfate), concentrate and crystallize with xylenes to give the desired compound (1.02 g, 50%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07745438B2uspto-grants-2010_06