Reaktion #537051

ord-119c8373af7844c090a699bc5e9cf13f

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas refluxed under an atmosphere of carbon monoxide (10 atm) overnight
  2. 2
    EinengenThe reaction was concentrated under reduced pressure
  3. 3
    Sonstigethe residue was purified by column chromatography on silica gel (petroleum ether/EtOAc 80:1)

Vorschrift

A mixture of 4-(tert-butoxycarbonylamino)-2,6-dichlorophenyl trifluoromethanesulfonate (14 g, 34 mmol), dppp (1.4 g, 3.4 mmol), Pd(OAc)2 (0.84 g, 3.4 mol) and Et3N (19.6 mL) in MeOH (112 mL) and DMF (224 mL) was refluxed under an atmosphere of carbon monoxide (10 atm) overnight. The reaction was concentrated under reduced pressure and the residue was purified by column chromatography on silica gel (petroleum ether/EtOAc 80:1) to give methyl 4-(tert-butoxy carbonylamino)-2,6-dichlorobenzoate (6.5 g, yield: 60%). 1H NMR (CDCl3, 400 MHz) δ 7.40 (s, 2H), 6.56 (brs, 1H), 3.94 (s, 3H), 1.51 (s, 9H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08486950B2uspto-grants-2013_07