Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 3,3,5-Trimethylcyclohexanone | HCID 13398 | — |
| Product | HCID 18505982 | HCID 18505982 | — |
Reaction Steps
The amount of the phenol (A) added after the conversion of 3,3,5-trimethylcyclohexanone (B) has reached 90 mol % or over is preferably such that the total molar amount of the phenol (A) added (the total phenol (A) consisting of the phenol (A) introduced in carrying out the pre-reaction, the phenol (A) dropped in the form of a liquid mixture with 3,3,5-trimethylcyclohexanone (B) in the reaction mixture and the phenol (A) added after the conversion of 3,3,5-trimethylcyclohexanone (B) has reached 90 mol % or over) is 5 to 10 times, especially 6 to 8 times, based on the molar amount of 3,3,5-trimethylcyclohexanone (B). When the amount of the phenol (A) added after the conversion of 3,3,5-trimethylcyclohexanone (B) has reached 90 mol % or over falls within the above range, not only can the rise of the viscosity of the reaction mixture be suppressed to thereby ensure efficient operation but also the desired 3,3,5-trimethylcyclohexylidenebisphenol can be obtained at high yield. The degree of conversion (%) of 3,3,5-trimethylcyclohexanone (TMC) is defined by the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06284931B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-820684487be84032ad195bf57f859856 |
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| Source note | uspto-grants-2001_09 |
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