HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487207Generated: October 31, 2026
N-bromobutanimide → Methyl 2-(bromomethyl)-4-nitrobenzoate
https://huagongshe.com/reaction/1487207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-methyl-4-nitrobenzoate | HCID 15088700 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl 2-(bromomethyl)-4-nitrobenzoate | HCID 15088701 | — |
Reaction Steps
2-methyl-4-nitrobenzoic acid methyl ester (696 mg, 3.57 mmol), azobisisbutyronitrile (58.6 mg, 0.357 mmol) and N-bromosuccinimide (785 mg, 4.46 mmol) were suspended in carbon tetrachloride (35 mL) in a sealed tube. The above mixture was flushed with nitrogen for 5 minutes and heated at 80° C. for 22 hours. After cooling, the solid was filtered off and the filtrate was concentrated to dryness to obtain the crude product methyl 2-(bromomethyl)-4-nitrobenzoate as a light-brown solid, which was used for the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428508B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-c34485451b3f434b867472e16d7846d4 |
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| Source note | uspto-grants-2016_08 |
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