HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038463Generated: October 25, 2026
Nitric Acid → Methyl 3-acetylamino-6-bromo-2-nitrobenzoate
https://huagongshe.com/reaction/1038463
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Methyl 5-acetamido-2-bromobenzoate | HCID 58891822 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-acetylamino-6-bromo-2-nitrobenzoate | HCID 11151255 | 62% |
Reaction Steps
To conc. sulfuric acid (150 mL), methyl 5-acetylamino-2-bromobenzoate (Reference Compound No. 1-(2), 18.5 g, 68.1 mmol) was added at 0° C. portionwise, and conc. nitric acid (150 mL) was added dropwise thereto over 1 hour. The reaction mixture was stirred for 30 minutes, poured into iced water (1 L), and then extracted with ethyl acetate (500 mL, 2 times). The organic layer was washed with water (1 L, 2 times), saturated aqueous sodium hydrogen carbonate solution (1 L), and saturated brine (1 L) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (13.4 g) as a yellow solid. (Yield 62%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08551991B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-d8512153a50b4293b2d8c3dd8b6ba5c0 |
|---|
| Source note | uspto-grants-2013_10 |
|---|