Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | P-Cresol | HCID 2879 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Methanediol, (2-methylphenyl)- | HCID 6451246 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67686069 | HCID 67686069 | — |
Reaction Steps
p-Cresol in an amount of 38.4 g (0.36 mole) and 35.0 g (0.25 mole) of xylene-α,α-diol were dissolved with heating, followed by addition of 0.15 g of methanesulfonic acid at 90° to 100° C. The reaction was carried out at 90° to 100° C. for 2 hours with stirring. After cooling, 100 ml of acetone was poured into the reaction solution. After dissolving, the reaction solution was poured into 2000 ml of water and stirred. After allowed to stand, a supernatant was removed by decantation. The residue was dissolved in 100 ml of acetone, followed by pouring into 2000 ml of water and stirring. After allowed to stand, a supernatant was removed by decantation. The residue was dried under reduced pressure to give 65.0 g of pale yellowish powdered crystals of p-cresol/1,4-dihydroxymethylbenzene polycondensate. Mw was about 6,700 and the degree of dispersion was 3.50 (GPC method, polystyrene standard).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06033826 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-b2a68e466a0047a1bafb557ae60ff3d6 |
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| Source note | uspto-grants-2000_03 |
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