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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 851673Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Carboxyethyl 2,3,4,6-tetra-O-acetyl-1-thio-alpha-D-mannopyranoside

https://huagongshe.com/de/reaction/851673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPropanoic acid, 3-iodo-HCID 8856—
EduktPotassium CarbonateHCID 11430—
EduktPotassium MetabisulfiteHCID 28019—
Edukt2-S-(2,3,4,6-tetra-O-acetyl-alpha-D-mannopyranosyl)-2-thiopseudourea hydrobromideHCID 22823287—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
Produkt2-Carboxyethyl 2,3,4,6-tetra-O-acetyl-1-thio-alpha-D-mannopyranosideHCID 2352446899,1%

Reaktionsschritte

A mixture of 2-S-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-thiopseudourea hydrobromide (1) (90 g, 0.185 mol), freshly crystallized 3-iodopropionic acid (37 g, 0.199 mol), potassium carbonate (29.6 g, 0.215 mol), and potassium metabisulfite (37 g, 0.167 mol) in acetone (150 ml) and water (150 ml) is stirred for 45 minutes at room temperature. Hydrochloric acid (5%, 700 ml) and chloroform (700 ml) are added to the mixture. The organic layer is separated and washed with water, dried, and evaporated in vacuo to an oil (80 g, quantitative yield) that is used, without further purification, for the preparation of 3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04386026
Quelldatensatzuspto-grants-1983_05
ORD IDord-f801664b6ce441f7bbdbcc7aa63ecf90
Quellennotizuspto-grants-1983_05