HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243362Generated: October 25, 2026
Sulfuric Acid → Methyl 3-bromo-5-nitrobenzoate
https://huagongshe.com/reaction/1243362
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Methyl 3-nitrobenzoate | HCID 69260 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Catalyst | HCID 178418844 | HCID 178418844 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-bromo-5-nitrobenzoate | HCID 239341 | 72% |
Reaction Steps
A mixture of methyl 3-nitrobenzoate (122 g, 674 mmol), silver sulphate (100 g, 320.7 mmol) and concentrated sulfuric acid (750 mL) was stirred mechanically and heated at 90° C. To this mixture was added bromine (37 mL), dropwise, over 2 h. The reaction was stirred another hour, cooled and filtered. The filtrate was mixed with 2 L water and 1 Kg crushed ice. The solid was filtered and dried to afford a mixture of the desired methyl ester and free acid hydrolysis product. The mixture was taken up into methanol (1 L), treated with 10 drops concentrated sulfuric acid and refluxed for 12 h. The reaction mixture was allowed to cool and the crystals that were deposited were collected and dried in a desiccator to afford 126 g (72% yield) of methyl 3-bromo-5-nitrobenzoate (EX-119A): 1H NMR (300 MHz, CDCl3) δ 8.65 (s, 1H), 8.44 (s, 1H), 8.37 (s, 1H), 3.94 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119094B1 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-19b2dd6100e14109b7c4f2fb640df9d7 |
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| Source note | uspto-grants-2006_10 |
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