Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-Methyl-5-(1,1,3,3-tetramethylbutyl)pyrocatechol | HCID 75716 | — |
| Reactant | 1,2-Epoxy-2-methyl-5-hexene | HCID 14740384 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15117839 | HCID 15117839 | 25% |
Reaction Steps
A mixture of 10.5 g (44 mmole) of 3-methyl-5-t-octylcatechol, 11 g (90 mmole) of 1,2-epoxy-2-methyl-5-hexene and 0.75 ml of piperidine was heated at 120° C., with stirring, under nitrogen, for 7 days. The reaction mixture was cooled and dissolved in ether (300 ml), and the resulting solution was washed with water, followed by 1N hydrochloric acid, followed by saturated sodium chloride solution. The washed ethereal solution was dried (MgSO4) and evaporated in vacuo, and the residue was purified by column chromatography on silica gel, eluting with chloroform. This afforded a 25% yield of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04935442 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-93f9faae348b4ad9975ec0ed4327b0c5 |
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| Source note | uspto-grants-1990_06 |
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