Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene Oxide | HCID 7276 | — |
| Reactant | 1,1,1,3,3,3-Hexafluoro-2-propanol | HCID 13529 | — |
| Reactant | L-Ascorbic Acid | HCID 54670067 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67266647 | HCID 67266647 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163939B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-7a25156f7ac949b99cb70cbe7cb831a6 |
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| Source note | uspto-grants-2012_04 |
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