Reacción #50909

ord-72041597c8174feb98f00887889851c6

Ecuación de reacción

C=Cc1ccc(OC(C)(C)C)cc1
p-t-butoxy styrene
COC(=O)C#CC(=O)OC
acetylene dicarboxylic acid dimethyl ester
c1ccc2ccccc2c1
naphthalene
Rendimiento 142.9%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otro200 ml, and then reacted at the temperature of 140° C. for 5 hours
  2. 2
    TemperaturaAfter cooling
  3. 3
    Otronitro benzene was removed under a reduced pressure, silica gel column chromatography (developing solvent n-hexane:acetic acid ethyl=9:1)
  4. 4
    Otrothus 40.78 g crude material was obtained

Procedimiento

p-t-butoxy styrene 35.25 g (0.2 mol) and acetylene dicarboxylic acid dimethyl ester 56.84 g (0.4 mol) were dissolved in nitrobenzene, 200 ml, and then reacted at the temperature of 140° C. for 5 hours. After cooling, nitro benzene was removed under a reduced pressure, silica gel column chromatography (developing solvent n-hexane:acetic acid ethyl=9:1) was performed to the residual, thus 40.78 g crude material was obtained. Further, 36.63 g (yield 57.9%) objective naphthalene compounds were obtained by recrystallizing through diisopropyl ether. Melt points were 82.0-83.0° C. This naphthalene compound's infrared absorption spectrum is indicated in FIG. 4.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06849367B2uspto-grants-2005_02