HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | alpha-Chloro-m-nitrotoluene | HCID 12078 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | Nitrobenzene | HCID 7416 | — |
Reaction Steps
A derivative of 3-nitrobenzyl chloride (IV) and a compound of the formula (V) are reacted in a solvent such as dimethylformamide, hexamethylphosphoramide, etc., in the presence of a hydrogen chloride acceptor such as KOH, NaH, etc., at a temperature in the range from -10° to 150° C., preferably from 0° to 80° C., for 0.1 to 20 hours, preferably 0.5 to 10 hours, to obtain a nitrobenzene derivative of the formula (VI). This nitrobenzene derivative is reduced into an aniline derivative (VII) by a conventional method, for example, by adding hydrazine hydrate to said nitrobenzene derivative in an alcohol and heating the solution under reflux in the presence of palladium-charcoal for 1 to 10 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04983209 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-a342a50516074b9c894e512fb4a9fdf0 |
| Source note | uspto-grants-1991_01 |