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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848279Generated: November 2, 2026

Methane → 4-Acetyl-2-methylbenzoic acid

https://huagongshe.com/reaction/1848279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Bromo-3-methylphenyl)ethanoneHCID 347124—
ReactantHCID 178418416HCID 178418416—
CatalystPalladiumHCID 23938—
CatalystTetrabutylammonium BromideHCID 74236—
Catalyst1,3-Bis(diphenylphosphino)propaneHCID 81219—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-Acetyl-2-methylbenzoic acidHCID 5343555490%

Reaction Steps

63.9 g (300 mmol) of 4′-bromo-3′-methylacetophenone, 256 g of toluene, 32 g of water, 45.5 g (330 mmol) of potassium carbonate, 9.66 g (30 mmol) of tetra(n-butyl) ammonium bromide, 1.45 g (water content 55.95% by weight) of activated charcoal supported 5% palladium and 0.372 g (0.90 mmol) of 1,3-bis(diphenylphosphino)propane were fed into a pressure-tight reactor, and reaction was performed at 120° for 7 hours by pressurizing with carbon monoxide at 0.8 MPa. After cooling the reaction solution to room temperature, inside of the reactor was purged with nitrogen, and then the pressure was reduced to atmosphere pressure. 224 g of water was added, and stirred for 30 minutes. Catalyst was filtered with Celite and the organic phase was separated. 43.8 g (420 mmol) of 35% hydrochloric acid was added to the water phase. The obtained slurry was filtered, and then dried under reduced pressure to obtain 48.1 g of 4-acetyl-2-methylbenzoic acid as white crystal (yield 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952175B2
Source datasetuspto-grants-2015_02
ORD IDord-7043597911674417ab46dd258298f053
Source noteuspto-grants-2015_02