Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Butane, 1,1'-thiobis[3-methyl- | HCID 10990 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (1R,2S,5R)-6,6-Dimethylbicyclo(3.1.1)heptane-2-methanol | HCID 117419 | — |
| Reactant | (-)-beta-Pinene | HCID 440967 | — |
| Reactant | HCID 178419188 | HCID 178419188 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (-)-cis-Myrtanol | HCID 11084102 | — |
Reaction Steps
Borane-diisoamyl sulfide (5.0 ml, 21 mmol) was dissolved in THF (20 ml) and (-)-β-pinene (8.86 g, 64 mmol), [α]23D=-20.8° (neat), 91% ee, was added at 0° C. The mixture was kept at room temperature for 1 h and oxidized by the addition of 3M sodium hydroxide (10 ml, 30 mmol) and 30% hydrogen peroxide (7 ml, 70 mmol) keeping the temperature during the addition below 30° C. and then stirring at room temperature for 3 h. The mixture was saturated with potassium carbonate, the THF layer was separated and the aqueous layer was extracted with diethyl ether (2×50 ml). The extracts were combined with the THF solution, dried over magnesium sulfate and distilled using a Widmer column to give a first fraction, 4.25 g, bp 45°-58° C./0.1 mm Hg composed of diisoamyl sulfide (77%) and cis-myrtanol (23%) and a second fraction 7.96 g (82%), bp 58°-60° C./0.1 mm Hg, n20D=1.4907, [α]°D=-19.4° (neat).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05567849 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-ed64b13e10ef4a3293adf617ddbf550e |
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| Source note | uspto-grants-1996_10 |
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