Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454577Generated: October 30, 2026

Citric Acid → 2-(5-Bromo-2-hydroxybenzamido)-4-phenylbenzoic acid

https://huagongshe.com/reaction/454577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 2-(2-acetoxy-5-bromobenzamido)-4-phenylbenzoateHCID 66990421—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
Product2-(5-Bromo-2-hydroxybenzamido)-4-phenylbenzoic acidHCID 5850896370.2%

Reaction Steps

Potassium carbonate (0.049 g) was added to a solution mixture of tert-butyl 2-(2-acetoxy-5-bromobenzamido)-4-phenylbenzoate (0.060 g) in methanol (1 mL) and dioxane (1 mL), followed by stirring at room temperature for 1 hour. A 10% aqueous solution of citric acid and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. Trifluoroacetic acid (5 mL) was added to the obtained residue, followed by stirring at room temperature for 2 hours. The solvent was evaporated under reduced pressure, and methanol was added to the obtained residue. The solid substance was collected by filtration to obtain 0.034 g of 2-(5-bromo-2-hydroxybenzamido)-4-phenylbenzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-665663a03fa442a098e0e2cb54e8f76f
Source noteuspto-grants-2013_07