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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865823Generated: October 30, 2026

Hydrogen Peroxide → (-)-cis-Myrtanol

https://huagongshe.com/reaction/865823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantButane, 1,1'-thiobis[3-methyl-HCID 10990—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant(1R,2S,5R)-6,6-Dimethylbicyclo(3.1.1)heptane-2-methanolHCID 117419—
Reactant(-)-beta-PineneHCID 440967—
ReactantHCID 178419188HCID 178419188—
SolventTetrahydrofuranHCID 8028—
Product(-)-cis-MyrtanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05567849
Source datasetuspto-grants-1996_10
ORD IDord-ed64b13e10ef4a3293adf617ddbf550e
Source noteuspto-grants-1996_10