HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64248Erstellt: 24. Oktober 2026
Sodium Bicarbonate → allyl 3,4,6-tri-O-benzyl-beta-D-glucopyranoside
https://huagongshe.com/de/reaction/64248
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Tri-O-benzyl-D-glucal | HCID 11742644 | — |
| Edukt | Propan-2-one--dichloromethane (1/1) | HCID 21584124 | — |
| Edukt | Potassium hydroxy sulfite | HCID 23707502 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | allyl 3,4,6-tri-O-benzyl-beta-D-glucopyranoside | HCID 11027377 | 50% |
Reaktionsschritte
3,4,6-tri-O-benzyl-D-glucal (7.2 g, 17.3 mmol) in CH2Cl2/acetone (2:1, 105 mL) and a saturated solution of NaHCO3 (100 mL) was added. The mixture was stirred vigorously while a solution of Oxone (21.2 g, 34.6 mmol) in water (150 mL) was added dropwise over 30 minutes. After 1.5 hours of vigorous stirring the layers were separated, and the aqueous layer was extracted with CH2Cl2 (2×150 mL). The organic solutions were combined, dried over MgSO4, filtered and concentrated. The residue was co-evaporated with toluene (3×10 mL), dissolved in allyl alcohol (25 mL) and stirred at room temperature overnight. The reaction mixture was purified on a silica gel column (80 g) using an ISCO automated chromatography system, eluting with a 0→60% gradient of ethyl acetate in heptane, to give allyl 3,4,6-tri-O-benzyl-β-D-glucopyranoside (4.2 g, 50%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09447133B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-bba88a93227143cebe8f3aba0f22b6a6 |
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| Quellennotiz | uspto-grants-2016_09 |
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