HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methyl-4-nitroaniline → 2-bromo-N-methyl-N-(4-nitrophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methyl-4-nitroaniline | HCID 7483 | — |
| Reactant | Lithium Carbonate | HCID 11125 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-bromo-N-methyl-N-(4-nitrophenyl)acetamide | HCID 22668375 | — |
Reaction Steps
23.5 g (0.15 mol) of N-methyl-4-nitroaniline are dissolved in 400 ml of dioxane and combined with 22.2 g (0.3 mol) of lithium carbonate. Then 32.2 g (0.18 mol) of bromoacetylbromide are added dropwise in such a way that the internal temperature does not exceed 33° C. After 18 hours' stirring the reaction solution is evaporated down to 100 ml, combined with 500 ml of water and stirred for 1 hour. The precipitate formed is suction filtered, washed with water and dried. The crude product is stirred in 400 ml of ethyl acetate at 40° C. Then the insoluble matter is filtered off, the solution is evaporated down and the solid residue is triturated with ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06638965B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-bea18bee3b6d4a8f80a41c8184565167 |
| Source note | uspto-grants-2003_10 |