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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547981Generated: October 31, 2026

2-Bromopropane → Methyl 2-(4-bromophenyl)-3-methylbutanoate

https://huagongshe.com/reaction/547981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantMethyl 2-(4-bromophenyl)acetateHCID 316783—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(4-bromophenyl)-3-methylbutanoateHCID 46855859—

Reaction Steps

The (4-bromophenyl)acetic acid methyl ester in the Step 1 and potassium t-butoxide (4.8 g, 1 eq) were dissolved in 200 ml DMF at 0° C. Isopropyl bromide (4 ml. 1 eq) was added into the mixture and stirred at room temperature for 3 hours. When the reaction was completed, the mixture was extracted 3 times with ethyl acetate and water, and washed with saline solution. After the organic layer was dried with anhydrous and the solvent was removed at low pressures, the target compound 2-(4-bromophenyl)3-methylbutyric acid methyl ester was obtained by separation and purification of the mixture using a column chromatography (ethyl acetate:n-hexane=1:10) (6.60 g, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939672B2
Source datasetuspto-grants-2011_05
ORD IDord-d6dda329598045ae8ef0c73881bba2ed
Source noteuspto-grants-2011_05