HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352791Generated: October 27, 2026
Acetyl bromide → 4-Bromo-2,3-dimethylpyridine 1-oxide
https://huagongshe.com/reaction/352791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | 2,3-Dimethyl-4-nitropyridine-N-oxide | HCID 148223 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Product | 4-Bromo-2,3-dimethylpyridine 1-oxide | HCID 58997427 | — |
Reaction Steps
To 2,3-Dimethyl-4-nitropyridine N-oxide (3.00 g) which had been cooled to 0° C., added was acetyl bromide (18.0 ml), followed by stirring at 50° C. for 20 minutes and then at 75° C. for 15 minutes. The reaction mixture was charged in ice water and neutralized with an aqueous solution of ammonium carbonate. The neutralized solution was separated using methylene chloride. The organic layer was dried over anhydrous sodium sulfate and the filtrate was concentrated, whereby a crudely purified product of 4-bromo-2,3-dimethylpyridine N-oxide was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06747023B1 |
|---|
| Source dataset | uspto-grants-2004_06 |
|---|
| ORD ID | ord-8c6fda6a51f14930bce16d968b15977c |
|---|
| Source note | uspto-grants-2004_06 |
|---|