HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-(Acetoxymethyl)-6-benzoylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-benzoyl-2-methylpyridine N-oxide | HCID 54523980 | — |
| Product | 2-(Acetoxymethyl)-6-benzoylpyridine | HCID 23337841 | — |
Reaction Steps
Acetic anhydride (6.6 ml) is heated to 115°, after which 6-benzoyl-2-methylpyridine N-oxide is added in portions over 1 hour. The mixture is then held at 115° for 1 hour after the addition. The reaction is poured onto ice and extracted with ether (3×). The combined ether phases are washed with sat. NaHCO3 (2×) and water until neutral, dried and stripped. The product is preparatory thin layer chromatographed, the least polar band giving 2-(acetoxymethyl)-6-benzoylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04223033 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-ceb4f06ac4b941f7bc5f4c7562ba27f0 |
| Source note | uspto-grants-1980_09 |