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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroacetyl chlorideHCID 6577—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-5-chlorobenzoic acidHCID 12476—
SolventAcetonitrileHCID 6342—
Product5-Chloro-2-((2-chloroacetyl)amino)benzoic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571921
Source datasetuspto-grants-1996_11
ORD IDord-a1de311ebc264719961cf4cbd214c1b8
Source noteuspto-grants-1996_11