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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351999Generated: November 2, 2026

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

https://huagongshe.com/reaction/1351999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantMethyl 4-bromo-2-methylbenzoateHCID 22031226—
ReactantHCID 178418416HCID 178418416—
Catalystpalladium(II) acetateHCID 167845—
CatalystPhosphine, (1-methylethylidene)bis[diphenyl-HCID 12091099—
SolventAcetonitrileHCID 6342—
Product4-(Methoxycarbonyl)-3-methylbenzoic acidHCID 1867300387%

Reaction Conditions

Temperature83 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217728B2
Source datasetuspto-grants-2007_05
ORD IDord-9f6d9c66e1c4473c8743dd7fdd13e16c
Source noteuspto-grants-2007_05