Pyridine → Naphthalene
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]=1Participants
Reactant 1
Product 1
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
- customa Mettler softening point of 250° C.
- customwas conducted at 100° C.
- filtrationfollowed by filtration with a 0.5 μm membrane
- filtrationfilter
- customto remove a pyridien-insoluble matter
- customThen, from the soluble matter, pyridine was removed
- customto obtain a pyrildine-soluble pitch
- customΔTg of 33° C. and Qi of not more than 1% by weight
Sources & evidence
- ORD record
- ord-7fecb5693a824bec87565e573f5220fa
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05643546
Reaction notes
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