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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1887778Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1887778

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAnilineHCID 6115—
EduktPotassium CarbonateHCID 11430—
Edukt2-Bromo-4-chlorobenzoic acidHCID 33126—
KatalysatorCopperHCID 23978—
KatalysatorHCID 178419072HCID 178419072—
LösungsmittelWaterHCID 962—
LösungsmittelHexaneHCID 8058—
LösungsmittelGlycol monoethyl etherHCID 8076—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Chloro-2-(phenylamino)benzoic acidHCID 61533472,4%

Reaktionsbedingungen

Temperatur135 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08501732B2
Quelldatensatzuspto-grants-2013_08
ORD IDord-7ea6a7c86e68421298eaa6618c2fac53
Quellennotizuspto-grants-2013_08