Reacción #2195508

ord-52c99107fc7f4ff0b166c399b8379d10

Ecuación de reacción

[Na+].[OH-]
NaOH
C1=CC2C3C=CC(C3)C2C1
dicyclopentadiene
C=CC(Cl)c1ccccc1
vinylbenzyl chloride
O=[N+]([O-])c1ccc(O)c([N+](=O)[O-])c1
2,4-dinitrophenol
Cl
hydrochloric acid
C=COCc1ccccc1
vinylbenzyl ether
Rendimiento 95.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroequipped with a thermoregulator, a stirrer, a cooling condenser, and a dropping funnel
  2. 2
    workup.DISSOLUTIONdissolved
  3. 3
    workup.STIRRINGthe whole was stirred at 75° C. for additional 4 hours
  4. 4
    OtroAfter the obtained reaction mixture
  5. 5
    workup.ADDITIONwas added
  6. 6
    LavadoAn organic layer was then washed with 300 g of distilled water three times
  7. 7
    OtroAfter methyl ethyl ketone was removed under reduced pressure
  8. 8
    Otroa reaction product was precipitated in 300 ml of methanol
  9. 9
    Otroto collect a solid matter
  10. 10
    Filtraciónthrough filtration, which
  11. 11
    Otrowas then dried at 50° C. in a vacuum oven

Procedimiento

45 g (0.25 equivalent) of a dicyclopentadiene skeleton phenolic resin (DPP-3H, special phenolic resin, available from Nippon Petrochemical Co., Ltd.), 38.1 g of vinylbenzyl chloride (CMS-AM; purity of 91%; 0.25 mol; m-/p-isomers: 50/50 wt % mixture; available from Seimi Chemical Co., Ltd.), 2.4 g of tetra-n-butylammonium bromide, 0.038 g of 2,4-dinitrophenol, and 200 g of methyl ethyl ketone were charged into a 1-liter four-necked flask equipped with a thermoregulator, a stirrer, a cooling condenser, and a dropping funnel and dissolved under stirring. 40 g of a 50 wt % aqueous solution of NaOH (NaOH purity of 95%, 0.475 mol) was added dropwise at 75° C. to the obtained solution over 20 minutes, and the whole was stirred at 75° C. for additional 4 hours. After the obtained reaction mixture was cooled to room temperature, the mixture was neutralized with 2N hydrochloric acid, and 100 g of toluene was added. An organic layer was then washed with 300 g of distilled water three times. After methyl ethyl ketone was removed under reduced pressure, a reaction product was precipitated in 300 ml of methanol to collect a solid matter through filtration, which was then dried at 50° C. in a vacuum oven to obtain a vinylbenzyl ether compound at an yield of 95%. The obtained compound is designated as Compound 19.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07514379B2uspto-grants-2009_04