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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110035Generated: October 26, 2026

Acetic Acid → 2-Amino-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/2110035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
ReactantBenzoic acid, 2-amino-5-iodo-HCID 72911—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantHCID 178418416HCID 178418416—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Amino-5-(methoxycarbonyl)benzoic acidHCID 13105036—

Reaction Conditions

Temperature80 °C

Reaction Steps

After dissolving 2-amino-5-iodobenzoic acid (4 mmol, 1052 mg) in DMF (10 ml) and MeOH (5 ml), NEt3 (3 eq, 1.67 ml) was added. Next, palladium acetate (0.1 eq, 90 mg) and dppp (0.1 eq, 165 mg) were added, carbon monoxide substitution was carried out, and the mixture was stirred at 80° C. for 5 hours. Upon completion of the reaction, acetic acid (2.5 ml) was added to suspend the reaction. Water (50 ml) was added, and extraction was performed with ethyl acetate (50 ml×3 times). The organic layer was washed with water (100 ml×2 times) and then dried over sodium sulfate. After concentration, a developing solvent (Hex/AcOEt=4/1→1/1) was used for purification by silica gel chromatography to obtain 2-amino-5-(methoxycarbonyl)benzoic acid. The compound was identified by LC-MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517875B2
Source datasetuspto-grants-2009_04
ORD IDord-048688c5d3694dddb090ba85c4bb8d4f
Source noteuspto-grants-2009_04