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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2110035Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2110035

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktTriethylamineHCID 8471—
EduktBenzoic acid, 2-amino-5-iodo-HCID 72911—
Edukt1,3-Bis(diphenylphosphino)propaneHCID 81219—
EduktHCID 178418416HCID 178418416—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Amino-5-(methoxycarbonyl)benzoic acidHCID 13105036—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07517875B2
Quelldatensatzuspto-grants-2009_04
ORD IDord-048688c5d3694dddb090ba85c4bb8d4f
Quellennotizuspto-grants-2009_04