HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433870Generated: October 25, 2026
Sodium Azide → 3,4,6-Tri-O-Acetyl-2-Azido-2-Deoxy-alpha-D-Glucopyranosyl Bromide
https://huagongshe.com/reaction/433870
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Tri-O-acetyl-D-glucal | HCID 688303 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3,4,6-Tri-O-Acetyl-2-Azido-2-Deoxy-alpha-D-Glucopyranosyl Bromide | HCID 10715609 | — |
Reaction Steps
A 1 L flask containing 400 mL of acetonitrile was charged with sodium azide (7.75 g, 119.2 mmol) and ceric ammonium nitrate (120.7 g, 219.4 mmol). The resulting suspension was cooled to −30° C. and a solution of tri-O-acetyl-D-glucal (20.75 g, 76.22 mmol) in 100 mL acetonitrile was added to it dropwise. The reaction mixture was stirred at −30° C. for 20 hours and then warmed to room temperature, taken up in 800 mL of diethyl ether and washed with water (3×250 mL). The organics were dried over magnesium sulfate, filtered, and the solvent removed in vacuo to yield an oil. This oil was placed in a 1 L flask containing 400 mL of acetonitrile and lithium bromide (33.53 g, 386.1 mmol) and stirred at room temperature for at least 4 hours. The solvent was removed in vacuo and the resulting residue was taken up in 400 mL of dichloromethane. The organic layer was washed with water (2×250 mL), dried over magnesium sulfate and filtered. The solvent was removed in vacuo to yield the title compound as a gold oil which was used directly as in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06670324B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-def47593b63f498ca072d2820590d911 |
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| Source note | uspto-grants-2003_12 |
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