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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225115Generated: October 30, 2026

Hydrochloric Acid → Propanoic acid, 2-(4-benzoylphenoxy)-2-methyl-

https://huagongshe.com/reaction/225115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzonitrileHCID 7505—
ReactantTetrahydrofuranHCID 8028—
Reactant2-(4-Bromophenoxy)-2-methylpropanoic acidHCID 344894—
ReactantHCID 178418373HCID 178418373—
ProductPropanoic acid, 2-(4-benzoylphenoxy)-2-methyl-HCID 16911477%

Reaction Steps

26 g (0.1 mole) of 2-[(para-bromo)-phenoxy]-2-methyl-propionic acid is dissolved in 200 cc of anhydrous THF and placed in a 500 cc flask. The mixture is cooled in an ice bath and 0.2 mole of methylmagnesium iodide (prepared in solution of THF) is added slowly. After this addition, the temperature is allowed to rise and the mixture stirred at ambient temperature for 11/2 hours. Then slowly and drop by drop a solution of 4.1 g (0.1 mole) of benzonitrile in 20 cc of THF is added and the mixture is stirred for 2 hours 30 minutes at ambient temperature. The reaction mixture is poured on to 500 cc of 10% hydrochloric acid, cooled by 500 g of ice, and vigorously stirred. The reaction mixture is extracted with ether and the ethereal phases are washed, dried and decolorised. The ether solvent is evaporated under vacuum and the oily residue placed in a desiccator under vacuum. 2-[(para-benzoyl)-phenoxy]-2-methylpropionic acid slowly crystallises (22 g). The yield is 77% and the melting point 130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235896
Source datasetuspto-grants-1980_11
ORD IDord-bf7c5187bb134c8fb10b4df812b5e49b
Source noteuspto-grants-1980_11