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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887778Generated: October 25, 2026

Hydrochloric Acid → 4-Chloro-2-(phenylamino)benzoic acid

https://huagongshe.com/reaction/1887778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnilineHCID 6115—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-4-chlorobenzoic acidHCID 33126—
CatalystCopperHCID 23978—
CatalystHCID 178419072HCID 178419072—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
SolventGlycol monoethyl etherHCID 8076—
SolventEthyl AcetateHCID 8857—
Product4-Chloro-2-(phenylamino)benzoic acidHCID 61533472.4%

Reaction Conditions

Temperature135 °C

Reaction Steps

To a solution of 2-bromo-4-chlorobenzoic acid (25.0 g, 106.0 mmol) in 2-ethoxyethanol (40 mL) was added copper powder (0.74 g, 11.6 mmol), copper (I) oxide (0.76 g, 5.3 mmol), potassium carbonate (15.8 g, 114.0 mmol) at room temperature under nitrogen. After stirring for 5 min., aniline (11.2 mL, 124 mmol) was added to the reaction mixture. The reaction mixture was heated at 135° C. for 48 hr. Completion of the reaction was confirmed by silica TLC (mobile phase; hexane:ethyl acetate=1:1; Rf=0.6). The reaction mixture was cooled to room temperature, poured into water (30 mL) with continuous shaking and was acidified with aqueous 1N HCl to form a precipitate. The mixture was stirred overnight at room temperature. The mixture was filtered through a sintered glass funnel. The solids were washed with water (2×100 mL). The obtained solids were dried under high vacuum to yield 4-chloro-2-phenylamino-benzoic acid (19.0 g, 72.3% crude yield). The crude product was used in the next step without further purification. MS calcd. for C13H10ClNO2 [(M+H)+] 247, obsd. 248.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501732B2
Source datasetuspto-grants-2013_08
ORD IDord-7ea6a7c86e68421298eaa6618c2fac53
Source noteuspto-grants-2013_08