Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Benzene, 1,4-diphenoxy- | HCID 520487 | — |
| Reactant | 4,6-Diaminoresorcinol Dihydrochloride | HCID 2733648 | — |
| Product | Benzoxazole | HCID 9228 | — |
Reaction Steps
Under nitrogen atmosphere, 1.00 g (4.69 mmoles) of 4,6-diaminoresorcinol dihydrochloride and 1.62 g (6.26 mmoles) of oxy-bis(4-benzoic acid) are mixed and 29.1 ml of 10-1 methanesulfonic acid solution is added. The mixture is stirred and heated to 95° C. for 24 hours and then cooled to 50° C. A 0.41-g (1.56-mmole) quantity of p-diphenoxybenzene is added and stirring is continued at 50° C. for 48 hours. The resulting copolymer is precipitated in aqueous potassium hydroxide in a blender, washed with water until neutral and dried to constant weight in a vacuum oven at about 50° C. Its inherent viscosity in concentrated sulfuric acid at 25° C. and about 0.2028 g/dL concentration is measured to be about 0.99 dL/g. Its inherent viscosity in methanesulfonic acid at about 0.05 g/dL concentration and about 25° C. is measured to be 4.42 dL/g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05110894 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-ddb2a0c760164d3ead94363f2530e4fc |
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| Source note | uspto-grants-1992_05 |
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