HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaminophen → {4-[(2,4-Dichlorobenzyl)oxy]phenyl}amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaminophen | HCID 1983 | — |
| Reactant | 2,4-Dichlorobenzyl chloride | HCID 7212 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | {4-[(2,4-Dichlorobenzyl)oxy]phenyl}amine | HCID 11579870 | — |
Reaction Steps
In ethanol, p-hydroxyacetoanilide is reacted with 2,4-dichlorobenzyl chloride in the presence of sodium ethoxide and the resultant 4-(2,4-dichlorobenzyloxy)-acetoanilide is treated with potassium hydroxide in ethanol, whereby 4-(2,4-dichlorobenzyloxy)-aniline is obtained as crystals melting at 70°-71° C. In a similar manner, the following compounds can be prepared from the corresponding substituted benzyl halide derivatives.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04148625 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-4c19737ec5074348aae7fcac049d1513 |
| Source note | uspto-grants-1979_04 |