HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16188Generated: October 26, 2026
Anthranilic Acid → 2-(4-Chloro-2-nitroanilino)benzoic acid
https://huagongshe.com/reaction/16188
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Anthranilic Acid | HCID 227 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Chloro-1-fluoro-2-nitrobenzene | HCID 67660 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1-Pentanol | HCID 6276 | — |
| Product | 2-(4-Chloro-2-nitroanilino)benzoic acid | HCID 12042391 | — |
Reaction Steps
A solution of 4-chloro-1-fluoro-2-nitrobenzene (20 g, 114 mmol) and anthranilic acid (17.4 g, 127 mmol) in pentanol (250 mL) was heated to 120° C. in a Dean-Stark apparatus. Copper (126 mg, 2 mmol) was added, followed by potassium carbonate (12.7 g, 92 mmol). The resulting reaction mixture was stirred at 120° C. for 0.5 h and at 140° C. for 2 h. Subsequently, water and 1N (aq.) NaOH were added to dissolve the product. Then, the pH was adjusted to pH 5 and the water layer was extracted with ethyl acetate (3×). The combined organic layers were washed with water and brine, dried and evaporated. Ethanol was added to the obtained product. The title compound (14.4 g, 43%) was collected by filtration of the ethanol mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737136B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-d3c13c07f87242a2ae82606b819cd6b5 |
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| Source note | uspto-grants-2010_06 |
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