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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389242Generated: November 1, 2026

Sodium Hydroxide → 2-Methyl-4-((2-methylbenzoyl)amino)benzoic acid

https://huagongshe.com/reaction/2389242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Methyl-N-(m-tolyl)benzamideHCID 95290—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product2-Methyl-4-((2-methylbenzoyl)amino)benzoic acidHCID 2519211765.8%

Reaction Conditions

Temperature3 °C

Reaction Steps

To a solution of 3-(2-methylbenzoylamino)toluene (50.0 g, 0.222 mole) in methylene chloride (50 mL) which is cooled to 3° C. is added aluminum chloride (88.8 g, 0.666 mole) under nitrogen atmosphere over a period of about 10 minutes. The mixture is cooled to 3° C., and thereto is added dropwise oxalyl chloride (25.2 mL, 0.289 mole) at 3-7° C. The mixture is stirred at 2-7° C. for 5 hours. After confirming the disappearance of the starting materials, the reaction mixture is diluted with methylene chloride (100 mL), and thereto is added ice water to quench the reaction. After distilling off methylene chloride, the resulting aqueous suspension is refluxed for 30 minutes and then cooled to room temperature. The resulting crystals are separated by filtration and the wet crystals are dried at 60° C. to give the crude product (58.33 g). To the crude product (29.17 g) are added 2.5 mol/L aqueous sodium hydroxide solution (400 mL) and toluene (100 mL), and insoluble materials are removed by filtration and then separated into two layers. The aqueous layer is washed twice with toluene (100 mL) and neutralized with 6 mol/L hydrochloric acid (300 mL). The precipitated crystals are separated by filtration and dried at 60° C. and then recrystallized from methanol (540 mL) to give the desired product (19.67 g, yield 65.8%, purity by HPLC 99.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273735B2
Source datasetuspto-grants-2012_09
ORD IDord-414c8eb31bd84c2e93cbda62e537901a
Source noteuspto-grants-2012_09