Title: Base catalysed methanolysis of 4-anilinomethylene-2-phenyl-2-oxazolin-5-one: Unexpected formation of N-benzoylaminoacetanilide
| dc.contributor.author | R.S. Singh | |
| dc.contributor.author | M.K. Singh | |
| dc.contributor.author | R.M. Singh | |
| dc.date.accessioned | 2026-02-06T10:36:59Z | |
| dc.date.issued | 2000 | |
| dc.description.abstract | The reaction of 4-anilinomethylene-2-phenyl-2-oxazolin-5-one 1 with 3.0 equivalents of sodium methoxide in methanol affords N-benzoylaminoacetanilide 3. Further, methyl 3-anilino-2-benzoylaminopropenoate 2 also affords product 3, when treated with sodium methoxide in methanol at reflux temperature. A plausible mechanism for this conversion has been proposed. | |
| dc.identifier.issn | 3764699 | |
| dc.identifier.uri | https://dl.bhu.ac.in/bhuir/handle/123456789/16680 | |
| dc.title | Base catalysed methanolysis of 4-anilinomethylene-2-phenyl-2-oxazolin-5-one: Unexpected formation of N-benzoylaminoacetanilide | |
| dc.type | Publication | |
| dspace.entity.type | Article |