HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Fluoro-2-methyl-6-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(4-fluoro-2-methyl-6-nitrophenyl)acetamide | HCID 54330341 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Fluoro-2-methyl-6-nitroaniline | HCID 10374842 | 94.3% |
Reaction Steps
A stirred solution of 22.4 grams (0.106 mole) of 5-fluoro-2-methylcarbonylamino-3-methyinitrobenzene, 100 mL of concentrated hydrochloric acid, and 100 mL of ethanol was heated at reflux for about 17 hours. The reaction mixture was cooled and poured into 500 grams of ice. The mixture was made basic with aqueous 50% sodium hydroxide. The resultant solid was collected by filtration and was thoroughly washed with water. The solid was dried at about 60° C. under vacuum, yielding 17.0 grams of 4-fluoro-2-nitro-6-methylaniline, mp 111°-113°C. The NMR spectrum was consistent with the proposed structure. The reaction was repeated to obtain more product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05874579 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-8ecadae982454a988d8eeb66f277872f |
| Source note | uspto-grants-1999_02 |