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HRID 1887778作成日:2026年10月27日

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

https://huagongshe.com/reaction/1887778

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物AnilineHCID 6115—
反応物Potassium CarbonateHCID 11430—
反応物2-Bromo-4-chlorobenzoic acidHCID 33126—
触媒CopperHCID 23978—
触媒HCID 178419072HCID 178419072—
溶媒WaterHCID 962—
溶媒HexaneHCID 8058—
溶媒Glycol monoethyl etherHCID 8076—
溶媒Ethyl AcetateHCID 8857—
生成物4-Chloro-2-(phenylamino)benzoic acidHCID 61533472.4%

反応条件

温度135 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08501732B2
出典データセットuspto-grants-2013_08
ORD IDord-7ea6a7c86e68421298eaa6618c2fac53
出典メモuspto-grants-2013_08