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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1105878Erstellt: 26. Oktober 2026

Triethylamine → 6-(5-Cholesten-3beta-yloxy)hexyl 2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranoside

https://huagongshe.com/reaction/1105878

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt6-(5-Cholesten-3beta-yloxy)hexyl iodideHCID 12805525—
Edukt2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranoseHCID 23238908—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-(5-Cholesten-3beta-yloxy)hexyl 2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranosideHCID 13171264361%

Reaktionsschritte

2,3,4-Tri-O-acetyl-1-thio-β-L-fucopyranose (10 mmol) is treated with 6-(5-cholesten-3β-yloxy)hexyl iodide (10 mmol) in dichloromethane (30 ml) containing triethylamine (10 mmol). The reaction takes place in 1 day at room temperature under nitrogen. The resulting solution is washed with distilled water (20 ml) and dried with anhydrous sodium sulfate. The filtered solution is concentrated to form a syrup which is put on a silica gel column and eluted with chloroform followed by 1.0% ethanol in chloroform. The fractions containing the title compound, as determined by thin layer chromatography, are pooled and evaporated to give the title compound in 61% yield [α]D -4° (c 1.5, chloroform).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04310505
Quelldatensatzuspto-grants-1982_01
ORD IDord-11d0510d869e4df58af621773eb555f4
Quellennotizuspto-grants-1982_01