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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698288Generated: October 31, 2026

Styrene Oxide → HCID 67266647, compound

https://huagongshe.com/reaction/1698288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStyrene OxideHCID 7276—
Reactant1,1,1,3,3,3-Hexafluoro-2-propanolHCID 13529—
ReactantL-Ascorbic AcidHCID 54670067—
SolventAcetonitrileHCID 6342—
ProductHCID 67266647HCID 67266647—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under an argon atmosphere, 4 ml of 1,1,1,3,3,3-hexafluoro isopropanol and 10 ml of acetonitrile were added to L-ascorbic acid (1.00 g), and further, styrene oxide (1.37 g) was added. The mixture was heated up to 70° C. and stirred for 48 hours, then, concentrated under reduced pressure, and 2.73 g of the resultant residue was subjected to silica gel column chromatography. Thereafter, it was eluted with chloroform/methanol/water(volume ratio:20/3/0.3) to obtain two elution fractions (first eluted fraction: 225 mg, later eluted fraction: 228 mg). Based on the measurement results of high resolution mass analysis, infrared absorption spectrum, 1H-NMR, 13C-NMR and specific optical rotation on the resultant elution fractions, it was confirmed that these are two 3-O-(2-hydroxy-1-phenylethyl) ascorbic acids which are in mutual stereoisomerism and both of them are represented by the following structural formula.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163939B2
Source datasetuspto-grants-2012_04
ORD IDord-7a25156f7ac949b99cb70cbe7cb831a6
Source noteuspto-grants-2012_04