Reaktion #595341

ord-11fa7d888c304aceb6bce33ccfc5a02c

Reaktionsgleichung

Cc1cc(-c2nc(CO)co2)ccc1Cl
compound
Cc1cc(-c2nc(CO)co2)ccc1Cl
[2-(4-Chloro-3-methylphenyl)-1,3-oxazol-4-yl]methanol
O=S(Cl)Cl
thionyl chloride
Cc1cc(-c2nc(CCl)co2)ccc1Cl
4-(Chloromethyl)-2-(4-chloro-3-methylphenyl)-1,3-oxazole

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
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 reactions

Vorschrift

136 mg (0.61 mmol) of the compound from Example 27A are suspended in 2 ml of dichloromethane. The suspension is cooled to 0° C., and 49 μl (0.67 mmol) of thionyl chloride are added slowly. The reaction solution is stirred at RT overnight. The solvent is then removed on a rotary evaporator. The residue is used without further purification in the subsequent reactions.

Quelle

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