Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Vinylphenol | HCID 62453 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Ethynylphenol | HCID 32758 | — |
Reaction Steps
The same crude p-vinylphenol as used in Example 1 was subjected to azeotropic distillation with toluene without being subjected to vacuum flash distillation, to reduce the water content to 0.038%. A polymerization reaction was conducted in the same manner as in Example 1 except that 28.8 g of acetonitrile was added to 32.3 g of the above-obtained fraction. The reaction mixture was purified by the same reprecipitation as in Example 1, and the resulting precipitate was dried to obtain 6.5 g of a yellowish brown poly(p-vinylphenol). The polymer had a weight-average molecular weight (Mw) of 20,400, a number-average molecular weight (Mn) of 11,500, a light transmittance at a wavelength of 248 nm, of 68.0%, a light transmittance at a wavelength of 450 nm, of 83.2%, and a glass transition temperature of 177° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258901B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-9756f22c3ac3484eaae81b76f10c3555 |
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| Source note | uspto-grants-2001_07 |
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