Reacción #2328970

ord-222881038fa349c48a097882e44f1f23

Ecuación de reacción

Cl
hydrochloric acid
C=CC(=O)OCCCCOC(=O)Cl
4-acryloyloxybutyl chloroformate
O=C(O)c1ccc2cc(O)ccc2c1
6-hydroxy-2-naphthoic acid
C=CC(=O)[O-].Cl
acrylate HCl
[Na+].[OH-]
sodium hydroxide
[Na+].[OH-]
sodium hydroxide
C=CC(=O)OCCCCOC(=O)Oc1ccc2cc(C(=O)O)ccc2c1
6-(4-acryloyloxybutoxycarbonyloxy)-2-naphthoic acid

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas kept between 0 and 5° C.
  2. 2
    FiltraciónThe resulting suspension was filtered
  3. 3
    Lavadothe resulting filtercake was washed with 3 l of water
  4. 4
    Otroafter drying
  5. 5
    Otrowere obtained

Procedimiento

The pH of a solution of 100 g (0.53 mol) of 6-hydroxy-2-naphthoic acid in a solvent mixture of 600 ml of water and 500 ml of DMF was adjusted to 10 with 10 percent sodium hydroxide solution at 0° C. 132 g (0.61 mol) of 4-acryloyloxybutyl chloroformate (prepared according to WO 97/00600 A2) was subsequently added dropwise over a period of 2 h, in the course of which the temperature was kept between 0 and 5° C. and the pH at 10 (±0.2 pH unit) by means of 10 percent sodium hydroxide solution. The resulting solution was subsequently diluted with 3 l of water/ice mixture and the pH was adjusted to 5 with concentrated hydrochloric acid. The resulting suspension was filtered, the resulting filtercake was washed with 3 l of water and, after drying, 165.8 g (87% of theory based on the pure acrylate derivative) of a beige-colored powder were obtained, which comprises the compound NAPA shown above and the corresponding acrylate/HCl adduct.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07670505B2uspto-grants-2010_03