Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Trimethylamine oxide | HCID 1145 | — |
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bis(1,2-dimethylpropyl)borane | HCID 192733 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Silane, trimethyl[[1-methyl-1-(2-propynyl)pentyl]oxy]- | HCID 10856810 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 12884304 | HCID 12884304 | — |
Reaction Steps
To a stirred solution of 400 ml of 0.5 M bis-(3-methyl-2-butyl)borane in glyme, prepared from sodium borohydride, 2-methyl-2-butene, and boronitrifluoride etherate as in Example 107, is added 63.7 g (0.30 moles) of 4-methyl-4-trimethylsilyloxy-1-octyne (Example 125) at -10° C. The solution is stirred at ambient temperature for 2.5 hours, cooled to -10° C, and treated during 30 minutes with 158 g (2.1 moles) of solid trimethylamine oxide with cooling. The mixture is stirred at ambient temperature for 2 hours and then poured into a stirred, ice-cold solution of 15% aqueous sodium hydroxide; the stirred mixture is treated immediately with a solution of 426 g (1.68 moles) of iodine in 1100 ml of tetrahydrofuran. After 4 hours the mixture is extracted with ether. The extract is washed successively with water, aqueous sodium thiosulfate, and brine and dried over magnesium sulfate. The extract is concentrated, and the residue is subjected to chromatography on silica gel with hexane to provide an oil, p.m.r. (CDCl3): δ 1.18 (singlet, 4-CH3 group).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04085272 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-b2a2a9f724d54a62bb9dc541ef51bd79 |
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| Source note | uspto-grants-1978_04 |
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