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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196284Generated: October 26, 2026

Methyl iodide → 2-[2-(Dimethylamino)phenyl]propanoic acid

https://huagongshe.com/reaction/1196284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-(2-(Dimethylamino)phenyl)acetic acidHCID 20466109—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product2-[2-(Dimethylamino)phenyl]propanoic acidHCID 54100613—

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 2-(2-dimethylaminophenyl)acetic acid (1.8 g) in dry tetrahydrofuran (10 cc) is added at 10° C. to a solution of lithium diisopropylamide (prepared by the action of a 1.6M solution (2.6 cc) of butyllithium in hexane on a solution of diisopropylamine (2.8 g) in dry tetrahydrofuran (30 cc) at 10° C.). The reaction mixture is stirred for 30 minutes at 20° C. and then for 30 minutes at 35° C. After cooling to 20° C., methyl iodide (0.63 cc) is added and the mixture is heated to 35° C. for 1 hour. It is cooled and diluted with water (20 cc) and ethyl acetate (100 cc). The aqueous phase is washed with ethyl acetate (100 cc), acidified to pH 5 with hydrochloric acid and extracted with ethyl acetate (2×100 cc). The organic phases are washed with water, dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa) to give (RS)-2-(2-dimethylaminophenyl)propionic acid (1 g) in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112988
Source datasetuspto-grants-1992_05
ORD IDord-e0d3677a4b1c44a9a1cd704c3d056b08
Source noteuspto-grants-1992_05