Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phloroglucinol | HCID 359 | — |
| Reactant | 2,4-Dihydroxybenzoic Acid | HCID 1491 | — |
| Reactant | 2,6-Bis((2-hydroxy-5-methylphenyl)methyl)-4-methylphenol | HCID 74181 | — |
| Reactant | 1,1,1-Tris(4-hydroxyphenyl)ethane | HCID 93118 | — |
| Reactant | 1,3,5-Tris(4-hydroxyphenyl)benzene | HCID 348148 | — |
| Reactant | Tri-(4-hydroxyphenyl)-phenyl methane | HCID 17820215 | — |
| Reactant | 2-(4-Hydroxyphenyl)-2-(2,4-dihydroxyphenyl)-propane | HCID 21885520 | — |
| Reactant | 4,6-Dimethyl-2,4,6-tri-(4-hydroxyphenyl)-heptane | HCID 21894433 | — |
| Product | Bisphenol P | HCID 630355 | — |
Reaction Steps
The polycarbonates may be branched by the incorporation of small quantities of polyhydroxy compounds, for example from 0.05 to 2.0 mole % (based on the bisphenols used). Polycarbonates of this type are described, for example, in German Offelengungsschrifts Nos. 1,570,533; 2,116,974; 2,113,347; in British Patent Nos. 885,442; 1,079,821 and in U.S. Pat. No. 3,544,514. Some of the polyhydroxy compounds which may be used are, for example, phloroglucinol, 4,6-dimethyl-2,4,6-tri-(4-hydroxyphenyl)-heptane, 1,3,5-tri-(4-hydroxyphenyl)-benzene, 1,1,1-tri-(4-hydroxyphenyl)-ethane, tri-(4-hydroxyphenyl)-phenyl methane, 2,2-bis-[4,4-(4,4'-dihydroxydiphenyl)-cyclohexyl]-propane, 2,4-bis-(4-hyroxyphenyl 4-isopropyl)-phenol, 2,6-bis-(2'-hydroxy-5-methylbenzyl)-4-methylphenol, 2,4-dihydroxybenzoic acid, 2-(4-hydroxyphenyl)-2-(2,4-dihydroxyphenyl)-propane, 1,4-bis-(4',4"-dihydroxytriphenylmethyl)-benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04202949 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-8980d9f4deb74ef1a4c82afe8f0d1948 |
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| Source note | uspto-grants-1980_05 |
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