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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025548Generated: October 25, 2026

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

https://huagongshe.com/reaction/1025548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactopyranoseHCID 2734154—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactitolHCID 1000752491%

Reaction Conditions

Temperature0 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729099B2
Source datasetuspto-grants-2014_05
ORD IDord-7df2f95ae1f34e4ca47f569ec9755811
Source noteuspto-grants-2014_05