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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025434Generated: October 26, 2026

Citric Acid → Methyl 2-{[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}benzoate

https://huagongshe.com/reaction/1025434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantDichloromethaneHCID 6344—
ReactantMethyl AnthranilateHCID 8635—
Reactant2-(Trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoateHCID 86676334—
SolventPyridineHCID 1049—
ProductMethyl 2-{[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}benzoateHCID 7123867992.2%

Reaction Steps

To a mixture of 2.09 g of 2-(trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoate and 20 mL of methylene chloride were added 982 mg of methyl 2-aminobenzoate and 2.10 mL of pyridine under ice-cooling, followed by stirring at room temperature for 15 hours. To the reaction mixture was added a 10% aqueous citric acid solution, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 2.61 g of methyl 2-{[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}benzoate as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729068B2
Source datasetuspto-grants-2014_05
ORD IDord-938a5f9b02ab4c829e97bcb206481ec6
Source noteuspto-grants-2014_05