Reaktion #477969

ord-7a2f96e1b8a347fe90d3fc257d9b83fa

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto reach room temperature
  2. 2
    WaschenThe organic phase was washed with water (2×100 mL), 1N NaOH until pH 6-7
  3. 3
    Trocknendried (Na2SO4)
  4. 4
    Filtrationfiltered
  5. 5
    Sonstigeevaporated in vacuo
  6. 6
    SonstigeThe residue was purified on silicagel (10 cm)
  7. 7
    SonstigePure fractions were collected from the pure EtOAc phase
  8. 8
    Sonstigeevaporated in vacuo

Vorschrift

To an ice cooled solution of the above crude 2,4-dichloro-1-methylsulfanylmethoxy-benzene (17 g) in DCM (200 mL) was added portion wise m-CPBA (13.8 g, 79.75 mmol) during 30 min. The resulting mixture was allowed to reach room temperature and stirring was continued for 16 hrs. The organic phase was washed with water (2×100 mL), 1N NaOH until pH 6-7, dried (Na2SO4), filtered and evaporated in vacuo. The residue was purified on silicagel (10 cm) using first heptane (1 L) followed by EtOAc:heptane (1:1) (1 L) and finally EtOAc as eluents. Pure fractions were collected from the pure EtOAc phase and evaporated in vacuo affording 10.1 g (69%) of 2,4-dichloro-1-methanesulfinylmethoxy-benzene as a solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08383683B2uspto-grants-2013_02