FIELD: chemistry.
SUBSTANCE: invention relates to a method of producing adamantane (tricyclo[3.3.1.13.7]decane) via isomerisation in two steps using endo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.02.6]decane) or endo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.02.6]decane) and exo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.02.6]decane) as the starting substance. The method involves the following steps: using one HF catalyst or two catalysts from HF catalysts and BF3 catalysts without a solvent, at the first step for isomerisation of endo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.02.6]decane) to exo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.02.6]decane); and using a HF catalyst and a BF3 catalyst without a solvent at the second step for isomerisation of exo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.02.6]decane) to adamantane (tricyclo[3.3.1.13.7]decane). The two-step isomerisation reaction takes place in a liquid phase, obtained in a reaction of a liquid-phase solution, and output of adamantane is controlled such that it is equal to or less than total solubility of adamantane in exo-tetrahydrodicyclopentadiene and solubility of adamantane in endo-tetrahydrodicyclopentadiene at the second isomerisation step.
EFFECT: use of the disclosed method enables to obtain adamantane without deposit thereof in form of a solid residue even without a solvent.
12 cl, 5 ex, 1 dwg
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Authors
Dates
2013-09-27—Published
2009-05-07—Filed