反応 #2195507

ord-af1290576fdf484881302e99b22f86c1

反応方程式

[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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他equipped with a thermoregulator, a stirrer, a cooling condenser, and a dropping funnel
  2. 2
    workup.DISSOLUTIONthe mixture was dissolved
  3. 3
    workup.ADDITIONwas added
  4. 4
    洗浄An organic layer was then washed with distilled water three times
  5. 5
    workup.DISTILLATIONAfter methyl ethyl ketone was distilled off under reduced pressure
  6. 6
    その他a reaction product was precipitated in methanol
  7. 7
    その他to collect a solid matter
  8. 8
    ろ過through filtration, which
  9. 9
    その他was then dried at 50° C. in vacuum

実験手順

45 g (0.25 equivalent) of a dicyclopentadiene skeleton phenolic resin (DPP-3H, special phenolic resin, available from Nippon Petrochemicals 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 four-necked flask equipped with a thermoregulator, a stirrer, a cooling condenser, and a dropping funnel, and the mixture was dissolved under stirring. 40 g of a 50 wt % aqueous solution of NaOH (NaOH, 0.48 mol) was added dropwise at 75° C. to the obtained solution over 20 minutes, and a reaction was further carried out at 75° C. for 4 hours. The obtained mixture in the flask was neutralized with 2N hydrochloric acid, and 100 g of toluene was added. An organic layer was then washed with distilled water three times. After methyl ethyl ketone was distilled off under reduced pressure, a reaction product was precipitated in methanol to collect a solid matter through filtration, which was then dried at 50° C. in vacuum to obtain a vinylbenzyl ether compound. The obtained compound is designated as Compound 11.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07514379B2uspto-grants-2009_04