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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600358Generated: November 1, 2026

Hydrochloric Acid → 2-Chlorobenzanilide

https://huagongshe.com/reaction/1600358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnilineHCID 6115—
Reactant2-Chlorobenzoic AcidHCID 8374—
ReactantThionyl ChlorideHCID 24386—
SolventTolueneHCID 1140—
Product2-ChlorobenzanilideHCID 2326593%

Reaction Steps

To a 500 ml four-necked flask equipped with a stirrer, a thermometer, and acondenser, 31.3 g (0.2 mol) of 2-chlorobenzoic acid and 180 g of toluene are placed. To the above mixture in the flask, 25.0 g (0.21 mol) of thionyl chloride is added dropwise over 30 minutes while stirring at a temperature of from 60° to 65° C. to be allowed to react with each other for about 30 minutes. To the above reaction mixture, a solution containing 27.9 g (0.3 mol) of aniline dissolved in 100 g of toluene is dropwise added to be allowed to react with each other at a temperature of from 70° to 75° C. for 30 minutes. After completion of the reaction, the reaction mixture is cooled to room temperature, and 70 g of a 5% by weight hydrochloric acid solution is added to the above mixture. The mixture is vigorously shaken and kept standing for separation of the toluene layer from the aqueous layer. Afterseparation of the toluene layer, it is condensed to precipitate white crystals, followed by recrystallization (in a water/methanol mixture of 3/7), to give 43.1 g of N-phenyl-2-chlorobenzamide (melting point: 116° to 117° C.). The yield of the product against 2-chlorobenzoic acid is 93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05744609
Source datasetuspto-grants-1998_04
ORD IDord-c3af8b2c36f34065ab4976b7c669ce9c
Source noteuspto-grants-1998_04