Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Hydrazine, 1,1-diphenyl-, hydrochloride (1:1) | HCID 10738 | — |
| Reactant | HCID 69294901 | HCID 69294901 | — |
| Catalyst | Methanesulfonic Acid | HCID 6395 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 131722565 | HCID 131722565 | — |
Reaction Steps
In a 100 mL single neck round bottom flask was weighed poly(bisphenol-A-benzophenone) (5.000 g, 11.50 mmol), 1,1-diphenylhydrazine hydrochloride (2.714 g, 12.30 mmol), THF (18 g) and N,N-dimethylacetamide (18 g). The flask was fitted with a condenser. The dark slurry was stirred with a magnetic stirrer to dissolve the starting materials. To the dark solution was added methanesulfonic acid (about 6 drops), and the solution heated to reflux . After stirring for about 4 hours, the orange polymer solution was precipitated in water, and chopped in a high speed blender. The yellow fibrous polymer was isolated by filtration, washed in boiling water (about 45 min.), filtered, washed in boiling methanol (about 45 min.), filtered and dried at about 100° C. for about 16 hours. The yield was about 5.29 g. The number average molecular weight of the polymer was about 11.8K.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350553B2 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-1a322bcf0a654b5d8c828b13a1803043 |
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| Source note | uspto-grants-2002_02 |
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