HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899394Generated: October 25, 2026
Hydrochloric Acid → 5-Chloro-2-((2-chloroacetyl)amino)benzoic acid
https://huagongshe.com/reaction/1899394
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-5-chlorobenzoic acid | HCID 12476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Chloro-2-((2-chloroacetyl)amino)benzoic acid | HCID 4179825 | — |
Reaction Steps
12.5 g (73 mmol) of 2-amino-5-chlorobenzoic acid are initially introduced into 500 ml of acetonitrile and treated with 9.0 g (80 mmol) of chloroacetyl chloride with stirring, the temperature being kept at 20°-25° C. (ice-bath). 22 g (0.16 mol) of finely pulverized potassium carbonate are then introduced and the mixture is stirred overnight at room temperature. The batch is adjusted to pH 2 with dilute hydrochloric acid and the acetonitrile is stripped off on a rotary evaporator. The precipitate is filtered off with suction and washed well with water. The crude product is treated with sodium bicarbonate solution and stirred. Insoluble matter is filtered off with suction and the filtrate acidified with dilute hydrochloric acid to pH 2. The precipitated product is filtered off with suction and dried. Yield: 7 g (77.3% of theory) M.p.: 188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05571921 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-a1de311ebc264719961cf4cbd214c1b8 |
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| Source note | uspto-grants-1996_11 |
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