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HRID 1025548Erstellt: 25. Oktober 2026

2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactopyranose → 2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactitol

https://huagongshe.com/reaction/1025548

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactopyranoseHCID 2734154—
EduktSodium borohydrideHCID 4311764—
LösungsmittelEthanolHCID 702—
Produkt2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactitolHCID 1000752491%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

2,3,4,6-Tetra-O-benzyl-D-galactopyranose (107 g) was dissolved in ethanol (0.6 L) and, whilst stirring at 0° C., sodium borohydride (31 g) was added. After stirring overnight TLC analysis indicated completion of the reaction. The ethanol solution was partitioned between water (3 L) and ether (1.5 L). The organic phase was dried (Na2SO4), filtered and concentrated. The resulting oil was purified by flash chromatography (gradient elution using 20→50% ethyl acetate/petroleum ether) and then crystallised from a mixture of ethyl acetate/petroleum ether to give 2,3,4,6-tetra-O-benzyl-D-galactitol (97 g, 91%) as a white solid. 1H NMR (CDCl3): δ 2.4 (1H, bs), 3.35 (1H, bs), 3.55 (2H, m), 3.8 (3H, m), 3.9 (2H, m), 4.1 (1H, m), 4.4-4.8 (8H, m, OCH2Ph), 7.2-7.4 (20H, m, ArH). Mass spectrum: m/z 543 (M+H)+ 565 (M+Na)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08729099B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-7df2f95ae1f34e4ca47f569ec9755811
Quellennotizuspto-grants-2014_05