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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 74853Erstellt: 24. Oktober 2026

Dichloromethane → 2,3,4,6-Tetra-O-benzoyl-beta-D-galactopyranosyl-(1->4)-1,2,3,6-tetra-O-benzoyl-D-glucopyranose

https://huagongshe.com/de/reaction/74853

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktBenzoyl chlorideHCID 7412—
Edukt(+)-LactoseHCID 440995—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelPyridineHCID 1049—
Produkt2,3,4,6-Tetra-O-benzoyl-beta-D-galactopyranosyl-(1->4)-1,2,3,6-tetra-O-benzoyl-D-glucopyranoseHCID 16158497—

Reaktionsschritte

Lactose (1.0 g, 2.92 mmol) was dissolved in dry pyridine (20 mL) at 0° C. DMAP (cat.) was added. Benzoyl chloride (2.5 equiv., 58 mmol, 6.8 mL) was added dropwise and the solution stirred at room temperature overnight. The solution was poured onto a mixture of ice-water and DCM. The organic layer was washed with NaHCO3(sat.) (×7), brine, H2SO4 (5%) (×2), followed by brine. The solution was dried (Na2SO4) and the solvent evaporated. The product was passed through a short silica plug to remove the remaining benzoyl chloride and the solvent was evaporated to yield 3.67 g (quantitative) of the white solid product which was reacted on without further purification or characterisation.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828952B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-05623dced9f84873b654e4d4a58e1b92
Quellennotizuspto-grants-2014_09