HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276014Generated: October 27, 2026
Hydrochloric Acid → ethyl 3-[N-(2-chlorobenzyl)acetylamino]-4-nitrobenzoate
https://huagongshe.com/reaction/276014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | alpha-Bromo-o-chlorotoluene | HCID 11905 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 3-acetylamino-4-nitrobenzoate | HCID 18315393 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 3-[N-(2-chlorobenzyl)acetylamino]-4-nitrobenzoate | HCID 18315549 | 81.6% |
Reaction Steps
A solution of 1.706 g of ethyl 3-acetylamino-4-nitrobenzoate in 12 ml of N,N-dimethylformamide were added 0.406 g of 60% sodium hydride while being cooled with ice, and the mixture was stirred at room temperature for 40 minutes. A solution of 1.806 g of 2-chlorobenzyl bromide in 10 ml of N,N-dimethylformamide was added thereto, and the mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into cold 1-N hydrochloric acid, and the mixed solution was extracted twice with ethyl acetate. The organic layer was washed with 1-N hydrochloric acid and then with water, and was dried. The solvent was distilled off under reduced pressure. The residue was purified through silica-gel column chromatography (eluent: a mixture of ethyl acetate and hexane at a ratio of from 1:10 to 1:4) to give 2.08 g of oily ethyl 3-[N-(2-chlorobenzyl)acetylamino]-4-nitrobenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06352985B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-86bbd89d855f442c8e9f95991ba4ccc3 |
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| Source note | uspto-grants-2002_03 |
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