HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864974Generated: October 30, 2026
Acetic Anhydride → 2-Chloro-3-nitro-6-acetoxymethylpyridine
https://huagongshe.com/reaction/864974
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Chloro-3-nitro-6-picoline-N-oxide | HCID 19417468 | — |
| Product | 2-Chloro-3-nitro-6-acetoxymethylpyridine | HCID 19417453 | — |
Reaction Steps
2-Chloro-3-nitro-6-picoline-N-oxide (1,6 g, 8.5 mmol) was dissolved in acetic anhydride (5 mL) and the solution was heated in a 60° C. oil bath for 3 hours. The solvents were removed under vacuum and the dark residue was partitioned between methylene chloride (30 mL) and saturated aqueous potassium carbonate (100 mL). The aqueous layer was re-extracted with more methylene chloride (2×40 mL) and the combined methylene chloride layers were dried with magnesium sulfate, filtered and evaporated under vacuum. The crude solid was dissolved in methylene chloride (SmL) and was loaded onto a silica gel column (E. Merck 60, 230-400 mesh, 2.5×24 cm). The column was eluted with methylene chloride collecting 8 mL fractions. Fractions 11-26 were combined and evaporated to give the title compound (0.42 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05565445 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-410ce3bbfe464423adcedbfbc5a627d6 |
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| Source note | uspto-grants-1996_10 |
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