HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxyacetanilide → HCID 22722095, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxyacetanilide | HCID 12124 | — |
| Reactant | Benzoic acid, 2-iodo-, methyl ester | HCID 69132 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 22722095 | HCID 22722095 | 55% |
Reaction Conditions
| Temperature | 180 °C |
|---|
Reaction Steps
To a stirred solution of methyl 2-iodobenzoate (10 g, 38.2 mmole) in dimethylacetamide (50 mL) was added 3-acetamidophenol (5 g, 33 mmole) and copper(I) oxide (2.5 g, 17 mmole), and the mixture was heated at reflux under argon (180° C. oil bath). After 24 h the reaction was cooled to RT and most of the solvent was distilled off. The remaining residue was purified by flash chromatography on silica gel (50% EtOAc/hexane) to give the crude title compound (4.95, 55%): MS (ES) m/e 286.2 (M+H)+. The title compound prepared in this way contained approximately 45% N,O-diarylated acetamidophenol as a contaminant: MS (ES) m/e 420.4 (M+H)+. The mixture was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06730684B1 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-1b1f33a9762048d4b8bf2650c870abff |
| Source note | uspto-grants-2004_05 |