HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610441Generated: October 29, 2026
Water → Phenyl 6-O-(4-azido-3-chlorobenzyl)-2,3,4-tri-O-benzyl-1-thio-D-glucopyranoside
https://huagongshe.com/reaction/610441
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-benzyl-1-thio-D-glucopyranoside | HCID 54027025 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Phenyl 6-O-(4-azido-3-chlorobenzyl)-2,3,4-tri-O-benzyl-1-thio-D-glucopyranoside | HCID 11354530 | 94% |
Reaction Steps
To a solution of phenyl 2,3,4-tri-O-benzyl-1-thio-D-glucopyranoside (3) (1.09 g, 2.00 mmol) in DMF (10 ml) was added sodium hydride (60% in oil, 96 mg, 2.40 mmol), and the resulting mixture was stirred at room temperature for 15 min. The reaction mixture was cooled to 0° C. and 4-azido-3-chlorobenzyl bromide (592 mg, 2.40 mmol) was added, which was followed by stirring at room temperature for 4 hr. Water (30 ml) was added and the mixture was extracted twice with ethyl acetate. The organic layers were combined, washed with 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=5:1) to give phenyl 6-O-(4-azido-3-chlorobenzyl)-2,3,4-tri-O-benzyl-1-thio-D-glucopyranoside (4) (1.33 g, yield 94%) as slightly yellow crystals.
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-baf9956c10ff45dd9d3ad2545077ee52 |
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| Source note | uspto-grants-1999_12 |
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