Reaktion #595351

ord-5f1b0992f6934014a33833ea9404f324

Reaktionsgleichung

COCOCc1nc(-c2ccc(Cl)cc2)oc1C(=O)O
compound
COCOCc1nc(-c2ccc(Cl)cc2)oc1C(=O)O
2-(4-Chlorophenyl)-4-[(methoxymethoxy)methyl]-1,3-oxazole-5-carboxylic acid
C[Si](C)(C)C=[N+]=[N-]
trimethylsilyldiazomethane
COCOCc1nc(-c2ccc(Cl)cc2)oc1C(=O)OC
Methyl 2-(4-chlorophenyl)-4-[(methoxymethoxy)methyl]-1,3-oxazole-5-carboxylate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe solvent is then removed on a rotary evaporator
  2. 2
    SonstigeThe residue is used without further purification in the subsequent reaction

Vorschrift

138 mg (0.52 mmol) of the compound from Example 42A are dissolved in 3 ml toluene and 2.5 ml of methanol. 0.4 ml (0.79 mmol) of a 2 M solution of trimethylsilyldiazomethane in hexane is then added dropwise. The mixture is stirred at RT for 10 min and the solvent is then removed on a rotary evaporator. The residue is used without further purification in the subsequent reaction.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09095582B2uspto-grants-2015_08