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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673546Generated: October 25, 2026

Hydrochloric Acid → 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoic acid

https://huagongshe.com/reaction/1673546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactanttert-butyl 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoateHCID 67344178—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoic acidHCID 5787934686%

Reaction Conditions

Temperature50 °C

Reaction Steps

1.0 mL of methanol and 0.5 mL of 2.0 mol/L aqueous sodium hydroxide were added to 1.0 mL of dioxane solution containing 20 mg of tert-butyl 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoate at room temperature and stirred at 50° C. for 30 minutes. Ethyl acetate and 1.0 mol/L hydrochloric acid were added after the reaction mixture was cooled to room temperature. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium chloride aqueous solution, and the solvent was evaporated under reduced pressure, Diisopropyl ether were added to toe obtained residue and a solid substance was separated by filtration to obtain 15 mg of 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoic acid as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-42cbf5a0ad8f41e8942a4333a253c2b3
Source noteuspto-grants-2011_08