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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1707950Erstellt: 25. Oktober 2026

Sodium Iodide → benzyl 3,5-di-O-benzyl-2-deoxy-1,4-dithio-d-erythro-pentofuranoside

https://huagongshe.com/reaction/1707950

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktBarium CarbonateHCID 10563—
Edukt3,5-di-O-benzyl-2-deoxy-4-O-methane-sulphonyl-L-threo-pentose dibenzyl dithioacetalHCID 15059960—
LösungsmittelAcetoneHCID 180—
Produktbenzyl 3,5-di-O-benzyl-2-deoxy-1,4-dithio-d-erythro-pentofuranosideHCID 11026498—

Reaktionsschritte

A suspension of 3,5-di-O-benzyl-2-deoxy-4-O-methanesulphonyl L-threo-pentose dibenzyl dithioacetal (29.4 g, 47.4 mmol), sodium iodide (74.0 g, 494 mmol), barium carbonate (148 g, 750 mmol) and dry acetone (1 L) was boiled under reflux for 42 hours. At the end of this time the suspension was filtered and the solids were washed with chloroform. The filtrate was sequentially washed with water, sodium thiosulphate solution (5%) and water, dried (magnesium sulphate) and evaporated. The resultant residue was applied to a silica gel column, eluted with hexane-ethyl acetate (9:1). Combination of the appropriate fractions gave the title product as a clear, slightly yellow, syrup, and recovered starting material.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05356882
Quelldatensatzuspto-grants-1994_10
ORD IDord-d92443e60c3b4f4b8c89f0c476ff585f
Quellennotizuspto-grants-1994_10