Reacción #595352

ord-2dadf170b3d6468882b6c489780934f2

Ecuación de reacción

COCOCc1nc(-c2ccc(Cl)cc2)oc1C(=O)OC
compound
COCOCc1nc(-c2ccc(Cl)cc2)oc1C(=O)OC
Methyl 2-(4-chlorophenyl)-4-[(methoxymethoxy)methyl]-1,3-oxazole-5-carboxylate
Cl
hydrochloric acid
COC(=O)c1oc(-c2ccc(Cl)cc2)nc1CO
Methyl 2-(4-chlorophenyl)-4-(hydroxymethyl)-1,3-oxazole-5-carboxylate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted three times with in each case 10 ml of diethyl ether
  2. 2
    SecadoThe combined organic phases are dried over magnesium sulfate
  3. 3
    Otrothe solvent is removed on a rotary evaporator
  4. 4
    OtroThe product obtained
  5. 5
    Otrois used without further purification in the subsequent reaction

Procedimiento

144 mg (0.52 mmol) of the compound from Example 43A are initially charged in 0.5 ml of methanol, and 0.13 ml of 4 N hydrochloric acid are added. 3 drops of conc. hydrochloric acid are then added. The reaction mixture is stirred at RT for 8 h. The mixture is then diluted with about 5 ml of water and extracted three times with in each case 10 ml of diethyl ether. The combined organic phases are dried over magnesium sulfate and the solvent is removed on a rotary evaporator. The product obtained is used without further purification in the subsequent reaction.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09095582B2uspto-grants-2015_08