HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6030Erstellt: 23. Oktober 2026
Benzylamine → 2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranose
https://huagongshe.com/de/reaction/6030
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzylamine | HCID 7504 | — |
| Edukt | 1,2,3,4-tetra-O-acetyl-5-thio-D-xylopyranose | HCID 10991244 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranose | HCID 23240188 | 47,3% |
Reaktionsschritte
22 ml (0.2 mol) of benzylamine are added under an inert atmosphere to a solution of 15 g (44.8.10-3 mol) of 1,2,3,4-tetra-O-acetyl-5-thio-D-xylopyranose in 450 ml of ether. After 7 hours at room temperature (15°-25° C.), the reaction mixture is concentrated under reduced pressure and the residue is dissolved in methylene chloride and washed with a 1N solution of hydrochloric acid, a saturated solution of ammonium chloride and then water. The solution obtained is dried over sodium sulfate and the solvent is evaporated off under reduced pressure. 6.2 g (yield: 47%) of the expected product are obtained after purification by chromatography on silica gel using a hexane/ethyl acetate mixture (3/2 v/v) as the eluent, and crystallization from an ethyl acetate/hexane mixture, said product having the following physical characteristics:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05246961 |
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| Quelldatensatz | uspto-grants-1993_09 |
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| ORD ID | ord-e496953e1a8048e29a65351a07d1384b |
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| Quellennotiz | uspto-grants-1993_09 |
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