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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063782Generated: October 25, 2026

Hydrochloric Acid → 2-(2,3-Dimethylphenoxy)-2-methylpropanoic acid

https://huagongshe.com/reaction/2063782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,3-DimethylphenolHCID 10687—
ReactantSodium HydroxideHCID 14798—
Reactant2-Bromo-2-methylpropanoic acidHCID 74924—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-(2,3-Dimethylphenoxy)-2-methylpropanoic acidHCID 153201345%

Reaction Conditions

Temperature50 °C

Reaction Steps

Sodium hydroxide (82.0 g, 2.05 mol) was added to a solution of methyl ethyl ketone (400 mL) containing 2,3-dimethylphenol (50.0 g, 410 mmol), and the mixture was stirred at 50° C. for 1 hour. After that, a solution of methyl ethyl ketone (200 mL) containing 2-bromo-2-methylpropionic acid (103 g, 615 mmol) was added thereto, and the mixture was stirred at 50° C. for 4 hours. After cooled to room temperature, the reaction solution was distributed by adding water and diethyl ether. 6N hydrochloric acid was added to the aqueous layer to be acidic, and then extraction was performed using ethyl acetate. The extract was washed with saturated saline, and then dried using anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the obtained residue was purified by silica gel chromatography (hexane-ethyl acetate 95:5 to 50/50) to give 38.3 g of the title compound (yield: 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288390B2
Source datasetuspto-grants-2012_10
ORD IDord-05ac9e0818184a36b03892f6a79883e2
Source noteuspto-grants-2012_10