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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 74852Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/74852

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktBenzoyl chlorideHCID 7412—
EduktD-(+)-Cellobiose (CNP0226604.15)HCID 10712—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelPyridineHCID 1049—
Produkt2,3,4,6-Tetra-O-benzoyl-beta-D-glucopyranosyl-(1->4)-1,2,3,6-tetra-O-benzoyl-D-glucopyranoseHCID 13173186122%

Reaktionsschritte

Cellobiose (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 740 mg (22%) 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-087f015a0871459db1217c26ee50654b
Quellennotizuspto-grants-2014_09