Reacción #2389077

ord-c847674200be4e1bba461e7f93b851ad

Ecuación de reacción

Cl
hydrochloric acid
COc1ccc2cc(C(C)=O)ccc2c1Br
2-acetyl-5-bromo-6-methoxynaphthalene
CCCCOC(C)=O
n-butyl acetate
C[O-].[Na+]
sodium methoxide
COc1ccc2cc(C(O)=CC(C)=O)ccc2c1Br
product
COc1ccc2cc(C(O)=CC(C)=O)ccc2c1Br
4-(5-Bromo-6-methoxy-2-naphthyl)-4-hydroxybut-3-en-2-one

Disolventes

Condiciones de reacción

Temperatura
65°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroequipped with refrigerator and stirrer
  2. 2
    workup.ADDITIONare added
  3. 3
    Otrogoes up to 25° C.
  4. 4
    TemperaturaThe reaction mixture is then cooled to 0°÷5° C.
  5. 5
    workup.WAITkept at this temperature for one hour
  6. 6
    FiltraciónThe solid is filtered
  7. 7
    Lavadoabundantly washed with water on the filter
  8. 8
    Lavadowashed with butyl acetate
  9. 9
    Otrodried in oven under vacuum

Procedimiento

50 Grams (0.179 moles) of 2-acetyl-5-bromo-6-methoxynaphthalene and 200 ml of n-butyl acetate are placed in a flask equipped with refrigerator and stirrer and, under stirring and at the temperature of 15° C., 14.5 g (0.268 moles) of sodium methoxide are added. The temperature of the reaction mixture goes up to 25° C. and is kept at this value for 30 minutes, then the mixture is warmed at 65° C. for one hour, is added with 100 ml of water and is brought to pH 4 by adding a concentrated aqueous solution of hydrochloric acid. The reaction mixture is then cooled to 0°÷5° C. and kept at this temperature for one hour. The solid is filtered, abundantly washed with water on the filter, then washed with butyl acetate and dried in oven under vacuum obtaining 53 g of product with a yield equal to 92%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE037813E1uspto-grants-2002_08