HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-Bromo-N-methyl-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Benzenamine, N-methyl-2-nitro- | HCID 69157 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromo-N-methyl-2-nitroaniline | HCID 258042 | 93.1% |
Reaction Steps
Pouring 60 milliliter of acetic acid over 5.0 g (33 mmol) of N-methyl-2-nitroaniline and 5.9 g (33 mmol) of N-bromosuccinimide, the resultant solution was refluxed with heating for 7 hours. After completion of the reaction, the reacted solution was poured into 500 milliliter of water, and precipitated solids were separated with filtration. Dissolving the resultant solids into ethyl acetate, the resultant solution was dried with the use of magnesium sulfate. After filtration, the solvent was removed by distillation under reduced pressure, and after drying the solids under reduced pressure at room temperature, 7.1 g of 4-bromo-N-methyl-2-nitroaniline as orange solids were obtained (yield: 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08097349B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-f90601c1bdb344d6b84112a3453fbf50 |
| Source note | uspto-grants-2012_01 |