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HRID 991148Erstellt: 26. Oktober 2026

Bromotriphenylmethane → 2-[1-[[(2S,3R,4R,5S,6R)-4,5-dihydroxy-2-phenylmethoxy-6-(trityloxymethyl)oxan-3-yl]amino]ethylidene]-5,5-dimethylcyclohexane-1,3-dione

https://huagongshe.com/reaction/991148

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromotriphenylmethaneHCID 11692—
Edukt2-[1-[[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-phenylmethoxyoxan-3-yl]amino]ethylidene]-5,5-dimethylcyclohexane-1,3-dioneHCID 178464538—
LösungsmittelDimethylformamide pyridineHCID 21954950—
Produkt2-[1-[[(2S,3R,4R,5S,6R)-4,5-dihydroxy-2-phenylmethoxy-6-(trityloxymethyl)oxan-3-yl]amino]ethylidene]-5,5-dimethylcyclohexane-1,3-dioneHCID 17846453766,9%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of Benzyl 2-Deoxy-2-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethylamino]-α-D-glucopyranoside (100 mg, 0.23 mmol), triphenylmethylbromide (149 mg, 0.46 mmol) in DMF/pyridine 1:1 (2 ml) was stirred at 100° C. for 15 h. The reaction mixture was evaporated, the residue was taken up in CHCl3 (10 ml), washed with water (3 ml), dried over MgSO4 and concentrated. The residue was purified by chromatography using CHCl3/MeOH 10:1 as the mobile phase to give Benzyl 2-Deoxy-2-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethylamino]-6-O-triphenylmethyl-α-D-glucopyranoside (14) (104 mg, 64%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06462183B1
Quelldatensatzuspto-grants-2002_10
ORD IDord-5cf03e04292e47499f6c253e6854a1b9
Quellennotizuspto-grants-2002_10