HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 6-benzoyl-2-methylpyridine N-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Benzoyl-6-methylpyridine | HCID 12623268 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-benzoyl-2-methylpyridine N-oxide | HCID 54523980 | — |
Reaction Steps
The 6-benzoyl-2-methylpyridine (3.9 g, 21 mmol), in 20 ml CHCl3, is added over 1 hour to 4.2 g (21 mmol) m-chloroperbenzoic acid (in 50 ml CHCl3). The temperature is kept below 25° as the mixture is stirred overnight. The reaction is diluted with CHCl3, washed with sat. NaHSO3, water, 20% NaHCO3 (2×) and then water, dried, stripped and finally titrated with hexane/ethyl acetate to give 6-benzoyl-2-methylpyridine N-oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226872 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-016cff6a9b3444f99a2e76f84011cf1b |
| Source note | uspto-grants-1980_10 |