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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453386Generated: October 26, 2026

Tributylamine → 5-(Methoxycarbonyl)-2-methylbenzoic acid

https://huagongshe.com/reaction/453386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
ReactantTriphenylphosphineHCID 11776—
ReactantCesium acetateHCID 5152919—
ReactantMethyl 3-bromo-4-methylbenzoateHCID 7015747—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-(Methoxycarbonyl)-2-methylbenzoic acidHCID 22999486—

Reaction Conditions

Temperature90 °C

Reaction Steps

A pressure vessel was charged with methyl 3-bromo-4-methylbenzoate (5.0 g, 22 mmol), DMF (20 ml), water (1.25 ml) and tributylamine (8 ml, 34 mmol). Cesium acetate (2.1 g, 11 mmol) was then added and the flask was purged with N2. Palladium acetate (0.25 g, 1.0 mmol) and triphenylphosphine (2.9 g, 11 mmol) were added and the flask was purged with CO gas. The reaction mixture was then heated at 90° C. under 20 psi of CO gas with vigorous stirring overnight. The reaction mixture was diluted with 50 mL of toluene and extracted with saturated NaHCO3 (3×50 ml). The combined aqueous layer was washed with EtOAc (10 mL), then acidified using 2 N HCl to pH 5. The volume was reduced to about 50 mL and the resulting precipitate was collected by filtration, washed with water and dried to give 5-(methoxycarbonyl)-2-methylbenzoic acid as a white solid. MS (ESI, pos. ion) m/z: 193.1 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492404B2
Source datasetuspto-grants-2013_07
ORD IDord-bb0fa4e87e7a423db7dc22bc87ac3ecb
Source noteuspto-grants-2013_07