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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238291Generated: October 31, 2026

Aniline → HCID 24762556, compound

https://huagongshe.com/reaction/2238291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant2-Amino-5-chlorobenzoic acidHCID 12476—
ReactantSodium Phosphate, DibasicHCID 24203—
Reactant4-t-Butylbenzenesulfonyl chlorideHCID 139882—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 24762556HCID 2476255687%

Reaction Steps

2-Amino-5-chlorobenzoic acid (200 g, 1.17 mol) was added to a solution of sodium hydrogen phosphate (497 g, 3.50 mol) in water (2.4 L) at 70° C. and was stirred until homogeneous (˜10 min). 4-tert-Butylbenzenesulfonyl chloride (353 g 1.52 mol), dissolved in 800 mL p-dioxane, was added to the stirring aniline solution in a steady stream over a ½ hour period via a 1 liter addition funnel. The resultant mixture was stirred at 70° C. overnight. The following day, upon LCMS verification of consumption of the aniline, the reaction mixture was divided into two equal portions for ease of handling. Each portion was poured in a slow stream into two liters of rapidly stirring 2 M HCl/H2O in a four liter Erlenmeyer flask. The resultant precipitate was collected by vacuum filtration and washed well with water. The precipitate from each portion were subsequently combined and dried in vacuo to afford 320 g 2-(4-tert-butyl-benzenesulfonylamino)-5-chloro-benzoic acid as an off-white solid (87% yield): HPLC retention time=2.76 minutes (Agilent Zorbax SB-C18, 2.1×50 mm, 5μ, 35° C., using a 1 mL/min flow rate, a 2.5 minute gradient of 20-100% B with a 1.1 minute wash at 100% B (A=0.1% formic acid/5% acetonitrile/94.9% water, B=0.08% formic acid/5% water/94.9% acetonitrile)); MS (ES) M+H expected 368.0, found 368.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718683B2
Source datasetuspto-grants-2010_05
ORD IDord-be2d0157ad784776b42d429c1925d511
Source noteuspto-grants-2010_05