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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183838Generated: October 27, 2026

Hydrochloric Acid → 2,5-Dimethylphenylacetic acid

https://huagongshe.com/reaction/1183838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Methyl-2-butanolHCID 6405—
ReactantSodium HydroxideHCID 14798—
ReactantBenzene, 2-(chloromethyl)-1,4-dimethyl-HCID 69987—
ReactantHCID 178418416HCID 178418416—
CatalystBis(triphenylphosphine)palladium chlorideHCID 84124—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
Product2,5-Dimethylphenylacetic acidHCID 8361587.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a 1000 ml autoclave, 70.0 g the said rectified 2,5-dimethylbenzyl chloride, 137.5 g triethylamine, 0.3 g palladium(II)bis(triphenylphosphine) dichloride, 81 g water and 168.0 g tert-pentanol are added. Nitrogen is inflated to replace the air for three times and the temperature is raised to 70° C. At 70° C.˜75° C., carbon monoxide is inflated until the pressure is not decreasing. After the reaction has finished, it is cooled to 40° C., then the pressure is relieved, and nitrogen is inflated to replace the air for three times again, the reaction solution is transferred into a 1000 ml four-neck flask and then 120.0 g 30% liquid caustic soda is added under the protection of nitrogen, which is stirred for 1 h at 60° C., then standing for layering. The upper layer is organic layer and the lower layer is water layer. 57.6 g 36% hydrochloric acid is added dropwise into the water layer until pH=1. The solution is kept warm for 1 h and filtered, dried under vacuum to give 64.4 g 2,5-dimethylphenylacetic acid (87.2% yield). Finally, small amount of heavy metal capture agent and flocculant can be added into the filtrate and filtered again to give the catalyst. The gained catalyst after filtering can be recycled and reused.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664424B2
Source datasetuspto-grants-2014_03
ORD IDord-205f98a9fc20407a824161b6c1c4f794
Source noteuspto-grants-2014_03