HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273836Generated: October 26, 2026
Diethyl Ether → 5-bromo-2-[(2-chlorophenyl)methyl]amino-3-nitrobenzoic Acid
https://huagongshe.com/reaction/273836
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chlorobenzylamine | HCID 66648 | — |
| Reactant | 2,5-dibromo-3-nitrobenzoic Acid | HCID 19351552 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-bromo-2-[(2-chlorophenyl)methyl]amino-3-nitrobenzoic Acid | HCID 19358545 | 61.5% |
Reaction Steps
A suspension of 2,5-dibromo-3-nitrobenzoic acid (10.76 g, 0.0331 mol) in toluene (100 mL) was placed under argon, treated with 2-chlorobenzylamine (14.06 g, 0.0993 mol) and the mixture was brought to reflux. A clear, red solution resulted and the solution was refluxed for 24 hours, cooled, poured into 5% sodium hydroxide solution (600 mL) and ether (100 mL). The insoluble material was filtered off, the layers separated and the aqueous phase was added to the insoluble material and acidified with 10% hydrochloric acid solution. The separated crystalline product was collected, washed with water and the solid was crystallized from a large volume of methanol to provide 7.85 g (61.5%) of the yellow crystalline 5-bromo-2-[(2-chlorophenyl)methyl]amino-3-nitrobenzoic acid; mp 159°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387601 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-630a5772fbe442e79cef8b0a39a8d6c6 |
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| Source note | uspto-grants-1995_02 |
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