Pyridine → Naphthalene

HRID 1450122Notes

Reaction equation

HRID 1450122 reaction equation
N1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>B(F)(F)F>[CH:2]1[C:6]2[C:6](=[CH:2][CH:3]=[CH:4][CH:5]=2)[CH:5]=[CH:4][CH:3]=1

Participants

3

Reagents, catalysts & solvents 1

Procedure

Naphthalene was polymerized at a temperature of from 200° to 400° C. in the presence of a HF.BF3 catalyst to obtain a pitch which had an optical anisotropy of 100% as observed under a polarization microscope, an optical anisotropic structure of a "rough flow type", a Mettler softening point of 250° C. and an elemental composition as analyzed of C: 94.8 wt % and H: 5.2 wt %. This pitch was finely pulverized. Then, pyridine (solubility parameter: 10.6) was added in an amount of 200 ml to 5 g of this pitch, and extraction was conducted at 100° C., followed by filtration with a 0.5 μm membrane filter to remove a pyridien-insoluble matter. Then, from the soluble matter, pyridine was removed to obtain a pyrildine-soluble pitch. The pitch had ΔTg of 33° C. and Qi of not more than 1% by weight.

Workup

  1. customa Mettler softening point of 250° C.
  2. customwas conducted at 100° C.
  3. filtrationfollowed by filtration with a 0.5 μm membrane
  4. filtrationfilter
  5. customto remove a pyridien-insoluble matter
  6. customThen, from the soluble matter, pyridine was removed
  7. customto obtain a pyrildine-soluble pitch
  8. customΔTg of 33° C. and Qi of not more than 1% by weight

Sources & evidence

ORD record
ord-81c47bba72d845929beca8ff04ee7873
Source dataset
uspto-grants-1997_02
Patent number
US05601794

Reaction notes

Loading…