HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetic Acid → Benzeneacetamide, N-(2-acetylphenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetic Acid | HCID 999 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2'-Aminoacetophenone | HCID 11086 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzeneacetamide, N-(2-acetylphenyl)- | HCID 218938 | — |
Reaction Steps
A mixture of o-aminoacetophenone (25 g.) and phenylacetic acid (25 g.) in anhydrous methylene dichloride (200 ml.) was prepared. To that mixture was added dicyclohexylcarbodiimide (40 g.) in portions of approx. 10 g. every 5 min. at ambient temperature. When the addition was completed the mixture was stirred for 4 hr. at ambient temperature. The mixture was then filtered, and the filtrate was evaporated in vacuo to dryness. The residue was crystallised from cyclohexane to give o-acetyl-N-(phenylacetyl)aniline, m.p. 78°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04607039 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-c30de0092d444a9b9d4cc6dd5c8c2e66 |
| Source note | uspto-grants-1986_08 |