HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925862Generated: October 28, 2026
Hydrochloric Acid → 4-Amino-3-chloro-2-fluoro-5-nitro-benzoic acid
https://huagongshe.com/reaction/1925862
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-Chloro-2,4-difluoro-5-nitrobenzoic acid | HCID 15549918 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Amino-3-chloro-2-fluoro-5-nitro-benzoic acid | HCID 21114182 | 85.8% |
Reaction Steps
Ammonium hydroxide solution (6.88 g, ˜30% in water, 58.9 mmol) is added to a solution of 3-chloro-2,4-difluoro-5-nitro-benzoic acid 2a (3.5 g, 14.7 mmol) in water (16 mL) at 0° C. with stirring. Upon completion of the ammonium hydroxide addition the reaction mixture is warmed to room temperature. After 5 hours the reaction mixture is cooled to 0° C. and concentrated HCl is carefully added until the pH of the reaction mixture is near zero. The solid is collected by filtration and washed with water and diethyl ether. The solids are transferred to a round bottom flask as a solution in MeOH and EtOAc and concentrated under reduced pressure to give 2.96 g of a yellow solid. The filtrate is partitioned between diethyl ether and water and the organic layer is washed with brine. The combined organic extracts are dried (Na2SO4) and concentrated under reduced pressure to give 0.65 g of product. Recovered a total of 3.61 g (104%) of pure desired product that is carried forward without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178693B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-e1d8d7dd8d3845568d0da42e3069cc0f |
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| Source note | uspto-grants-2012_05 |
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