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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119935Generated: October 31, 2026

EDTA disodium salt → (R,R)-Stilbene oxide

https://huagongshe.com/reaction/2119935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEDTA disodium saltHCID 8759—
ReactantSodium BicarbonateHCID 516892—
Reactanttrans-StilbeneHCID 638088—
ReactantPotassium hydroxy sulfiteHCID 23707502—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product(R,R)-Stilbene oxideHCID 18558373%

Reaction Conditions

Temperature0 °C

Reaction Steps

Aqueous Na2EDTA (1×10−4 M, 10 mL) and a catalytic amount of tetrabutylammonium hydrogen sulfate were added to a solution of trans-stilbene (0.18 g, 1 mmol) in acetonitrile (15 mL) with vigorous stirring at 0° C. A mixture of Oxone® (3.07 g, 5 mmol) and sodium bicarbonate (1.3 g, 15.5 mmol) was pulverized and a small portion of this mixture was added to the reaction mixture to bring the pH to >7. After 5 min, ketone 1 (0.77 g, 3 mmol) was added portionwise over a period of 1 h. Simultaneously, the rest of Oxone® and sodium bicarbonate was added portion was added portionwise over 50 min. After the completion of the addition of ketone 1, the reaction mixture was stirred for another 1 h at 0° C., diluted with water (30 mL), and extracted with hexanes (4×40 mL). The combined extracts were washed with brine, dried (Na2SO4), filtered, concentrated, and purified by flash chromatography [the silica gel was buffered with 1% triethylamine solution in hexane; hexane/ether (1/0 to 50/1, V/V) was used as the eluent] to afford trans-stilbene oxide as white crystals (0. 149 g, 73% yield, 95.2% ee).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686483B2
Source datasetuspto-grants-2004_02
ORD IDord-5dd64fa583ce4e688abb27d199c2fd45
Source noteuspto-grants-2004_02