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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactopyranose | HCID 2734154 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactitol | HCID 10007524 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729099B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-7df2f95ae1f34e4ca47f569ec9755811 |
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| Source note | uspto-grants-2014_05 |
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