Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyl borate | HCID 12712 | — |
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Reactant | 3,4-Dimethylcyclohexanol | HCID 97960 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 20495657 | HCID 20495657 | — |
Reaction Steps
n-butyl 3,4-dimethylcyclohexyl 2,6-di-t-butyl-4-methylphenyl borate was prepared by successively transesterifying tri-n-butyl borate with 2,6-di-t-butyl-4-methylphenol and 3,4-dimethylcyclohexanol. Tri-n-butyl borate (1 mole) and 2,6-di-t-butyl-4-methylphenol (1 mole) were heated, with stirring, to a temperature of 280° C. and n-butanol collected as a distillate. After seven hours 0.81 moles had been collected and a total of 0.82 moles collected after ten hours. After cooling the reaction vessel and adding 1 mole of 3,4-dimethylcyclohexanol, the reaction mixture was again heated to 280° C. for six hours, after which time a further 0.9 moles of n-butanol had been collected. Volatile components were then removed under reduced pressure (90° C./0.1 mm) to leave a viscous golden yellow liquid as product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04392973 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-a032efb2f125400d83e74f09b083d0aa |
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| Source note | uspto-grants-1983_07 |
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