Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | alpha-D-Glucopyranosyl bromide, tetraacetate | HCID 101776 | — |
| Edukt | Pterostilbene | HCID 5281727 | — |
| Katalysator | Benzyltriethylammonium bromide | HCID 165294 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Sodium Hydroxide | HCID 14798 | — |
| Produkt | HCID 69198447 | HCID 69198447 | — |
Reaktionsschritte
To a solution of acetobromo-α-D-glucose (48 mg, 0.11 mM) and benzyltriethylammonium bromide (13 mg, 0.04 mM) in chloroform was added a solution of pterostilbene (30 mg, 0.11 mM)) in 1.25 M (2.5 mL) of NaOH. The mixture was stirred at 60° C. for 5 h and after a second addition of 10 mg of acetobromo-α-D-glucose and 1.0 mL of NaOH) the mixture was stirred at 60° C. for additional 5 h. Ethyl acetate was added and the organic phase was washed with water. The crude mixture was purified using flash chromatography eluting with ethyl acetate/hexanes (3:2) and afforded (E)-2-(acetoxy-methyl)-6-(4-(3,5-dimethoxystyryl)phenoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08426369B2 |
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| Quelldatensatz | uspto-grants-2013_04 |
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| ORD ID | ord-1b30e9048f834828bdeaaab8034badb9 |
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| Quellennotiz | uspto-grants-2013_04 |
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