HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172768Generated: November 2, 2026
Pyridine → 4'-bromo-N-methyl-2'-nitrobenzanilide
https://huagongshe.com/reaction/1172768
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 4-Bromo-N-methyl-2-nitroaniline | HCID 258042 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4'-bromo-N-methyl-2'-nitrobenzanilide | HCID 23094078 | 97.7% |
Reaction Steps
6.8 g (29 mmol) of 4-bromo-N-methyl-2-nitroaniline were dissolved into 20 mL of pyridine. Furthermore, 5.0 g (35 mmol) of benzoyl chloride were added, and the whole was stirred under heating at 90° C. for 7 hours in an argon atmosphere. After the completion of the reaction, 200 mL of ethyl acetate were added, and the whole was washed with 10-mass % hydrochloric acid, 10-mass % K2CO3, and a saturated sodium chloride solution, and dried with magnesium sulfate. After filtration, the solvent was distilled off under reduced pressure, and the residue was purified by means of silica gel column chromatography to obtain 9.5 g of 4′-bromo-N-methyl-2′-nitro-benzanilide as a greenish white solid (96% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833632B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-6957104583bf4b228805b5b504a65efe |
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| Source note | uspto-grants-2010_11 |
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