Reaktion #476209

ord-c785325008a24a1a9f199a75b8555173

Reaktionsgleichung

COC(=O)c1sccc1CBr
Methyl 3-bromomethylthiophene-2-carboxylate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCOC(=O)CSc1ccc(O)cc1
compound
CCOC(=O)CSc1ccc(O)cc1
Ethyl (4-Hydroxyphenylsulfanyl)acetate
CCOC(=O)CSc1ccc(OCc2ccsc2C(=O)OC)cc1
captioned compound
Ausbeute 80.0%
CCOC(=O)CSc1ccc(OCc2ccsc2C(=O)OC)cc1
Methyl 3-(4-ethoxycarbonylmethylsulfanylphenoxymethyl)thiophene-2-carboxylate
Ausbeute 80.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISTILLATIONThe solvents were distilled off under a reduced pressure, water
  2. 2
    workup.ADDITIONwas added to the residue
  3. 3
    Extraktionthe product was extracted with ethyl acetate
  4. 4
    WaschenThe organic layer was washed with a saturated sodium chloride solution
  5. 5
    Trocknendried over anhydrous sodium sulfate
  6. 6
    workup.DISTILLATIONthe solvents were distilled off under a reduced pressure
  7. 7
    SonstigeThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1)

Vorschrift

Methyl 3-bromomethylthiophene-2-carboxylate (28.2 ml, 120 mmol) and potassium carbonate (36.6 g, 264 mmol) were added to a DMF (300 mL) solution of the compound obtained in Example 18 (28.1 g, 132 mmol), and the mixture was stirred overnight at room temperature. The solvents were distilled off under a reduced pressure, water was added to the residue, and the product was extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate, and the solvents were distilled off under a reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1), to give 35.1 g (80%) of the captioned compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08377967B2uspto-grants-2013_02