Reacción #577205
ord-94037b1dfdaf4369bd21fbcbdaefc412
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Otroto 45° C.
- 2Temperaturarefluxed for 2 hours
- 3Otrothe toluene layer was separated
- 4LavadoThe toluene layer was washed with 3% hydrochloric acid
- 5workup.DISTILLATIONa saturated sodium carbonate solution and water, and then toluene was distilled off
- 6workup.ADDITION20 g of sodium hydroxide, 500 mL of ethanol and 100 mL of water were added to the resulting residue
- 7Temperaturarefluxed for 2 hours
- 8OtroA residue obtained
- 9workup.DISTILLATIONby distilling ethanol
- 10Otroto obtain crystals
- 11OtroThe crystals thus obtained
- 12Filtraciónby filtering
- 13Otrowere recrystallized from ethanol
Procedimiento
12 g of ethyl hydroxybiphenylcarboxylate and 15 g of potassium hydroxide were added to 100 mL of ethanol, and stirred at 60° C. for 1 hour. After decreasing the temperature to 45° C., 15 g of 3-((tosyloxy)methyl)-3-ethyloxetane was added dropwise thereto, and then refluxed for 2 hours. Water and toluene were added thereto, and the toluene layer was separated. The toluene layer was washed with 3% hydrochloric acid, a saturated sodium carbonate solution and water, and then toluene was distilled off. 20 g of sodium hydroxide, 500 mL of ethanol and 100 mL of water were added to the resulting residue, and refluxed for 2 hours. A residue obtained by distilling ethanol off was put in 300 mL of 5% hydrochloric acid to obtain crystals. The crystals thus obtained by filtering were recrystallized from ethanol to obtain 8 g of 4-(3-ethyloxetane-3-ylmethoxy)biphenylcarboxylic acid (OX2), which had a melting point of 222 to 225° C.