HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610444Generated: November 1, 2026
Water → Phenyl 6-O-(4-azido-3-chlorobenzyl)-2,3,4-tri-O-(4-methoxybenzyl)-1-thio-beta-D-glucopyranoside
https://huagongshe.com/reaction/610444
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Azido-3-chlorobenzyl bromide | HCID 11482000 | — |
| Reactant | Phenyl 2,3,4-tri-O-(4-methoxybenzyl)-1-thio-beta-D-glucopyranoside | HCID 15433386 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Phenyl 6-O-(4-azido-3-chlorobenzyl)-2,3,4-tri-O-(4-methoxybenzyl)-1-thio-beta-D-glucopyranoside | HCID 15433387 | 79.1% |
Reaction Steps
To a solution of phenyl 2,3,4-tri-O-(4-methoxybenzyl)-1-thio-β-D-glucopyranoside (8) (1.25 g, 1.98 mmol) and 4-azido-3-chlorobenzyl bromide (584 mg, 2.37 mmol) in DMF (10 ml) was added sodium hydride (60% in oil, 95 mg, 2.37 mmol), and the resulting mixture was stirred at room temperature for 3 hr. Cold water was added and the mixture was extracted twice with ether. The combined ether layers were washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent; hexane:ethyl acetate=4:1) to give phenyl 6-O-(4-azido-3-chlorobenzyl)-2,3,4-tri-O-(4-methoxybenzyl)-1-thio-β-D-glucopyranoside (9) as white crystals (1.25 g, yield 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998595 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-43b604fd80b34958b88a63bb8a57dd36 |
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| Source note | uspto-grants-1999_12 |
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