HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297547Generated: October 30, 2026
Acetic Acid → 2,3,4,6-tetra-O-acetyl-5-thio-glucopyranose
https://huagongshe.com/reaction/1297547
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | (3R,4S,5S,6R)-6-(Acetoxymethyl)tetrahydro-2H-thiopyran-2,3,4,5-tetrayl tetraacetate | HCID 11654362 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,3,4,6-tetra-O-acetyl-5-thio-glucopyranose | HCID 11646270 | 88.2% |
Reaction Steps
To a solution of 1,2,3,4,6-penta-O-acetyl-5-thio-D-glucopyranose (34.0 g, 0.0837 mol) in N,N-dimethylformamide (300 mL), a mixture of methylhydrazine (6.70 mL, 0.120 mmol), acetic acid (15 mL, 0.120 mmol) and N,N-dimethylformamide (10 mL) was added in ice. After stirring at room temperature for 2.5 hours, 0.5M HCl (300 mL) was added to the reaction mixture in ice, which was then extracted twice with ethyl acetate (250 mL). The combined organic phases were washed sequentially with water (200 mL), saturated aqueous NaHCO3 (100 mL), water (100 mL) and saturated aqueous sodium chloride (100 mL), followed by addition of MgSO4 and activated charcoal (1 g). After filtration to remove the insoluble materials, the filtrate was concentrated under reduced pressure. The resulting residue was crystallized from isopropyl ether (70 mL) to give 2,3,4,6-tetra-O-acetyl-5-thio-gluco-pyranose (26.9 g, 88%) as a colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250522B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-92aff38ff7a84128afd18be6aa1f8d75 |
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| Source note | uspto-grants-2007_07 |
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