Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 393001Erstellt: 25. Oktober 2026

Water → 4-(Methoxycarbonyl)-3-methylbenzoic acid

https://huagongshe.com/reaction/393001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
EduktEthyl AcetateHCID 8857—
EduktMethyl 4-bromo-2-methylbenzoateHCID 22031226—
EduktHCID 178418416HCID 178418416—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorPhosphine, (1-methylethylidene)bis[diphenyl-HCID 12091099—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-(Methoxycarbonyl)-3-methylbenzoic acidHCID 1867300387%

Reaktionsbedingungen

Temperatur83 °C

Reaktionsschritte

A mixture of 4-bromo-2-methylbenzoic acid, methyl ester (22.59 g, 98.6 mmol), triethylamine (32.00 g, 316.2 mmol), palladium(II) acetate (0.56 g, 2.5 mmol), bis(diphenylphosphino)propane (1.04 g, 2.5 mmol) and water (32 mL, 1776.3 mmol) in acetonitrile (80 mL) was pressurized to 40 psi with carbon monoxide and the pressure was released. After six such cycles, the bottle was pressurized again and the contents were stirred at 83° C. for 3 h. The reaction mixture was cooled to room temperature and depressurized. Ethyl acetate (200 mL) was added. The solution was filtered and then extracted with water (2×300 mL). The combined aqueous layers were acidified with 12 M HCl to pH 0. The resulting mixture was extracted with ethyl acetate (2×300 mL). The combined organic layers were dried (MgSO4), filtered and evaporated to give 2-methylbenzene-1,4-dicarboxylic acid 1-methyl ester (16.57 g, 87%) as a white solid, mp 134-136° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06803384B2
Quelldatensatzuspto-grants-2004_10
ORD IDord-8d067f3f8e6544aa9eafb362d3fde711
Quellennotizuspto-grants-2004_10