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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896712Generated: October 30, 2026

Hydrochloric Acid → 2-(4-Bromophenyl)-2-methylpropanoic acid

https://huagongshe.com/reaction/896712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 2-(4-bromophenyl)-2-methylpropanoateHCID 3651431—
ReactantPotassium trimethylsilanolateHCID 23668039—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Bromophenyl)-2-methylpropanoic acidHCID 10933679101.1%

Reaction Steps

Methyl 2-(4-bromophenyl)-2-methylpropanoate (3.75 g, 14.6 mmol, prepared according to J. Org. Chem., 59:2620-2622(1994)) in 150 mL of THF was allowed to react with potassium trimethylsilanolate (2.62 g, 20.4 mmol) at ambient temperature, for 60 hours, with continuous stirring. The reaction was then diluted with water and DCM. The pH of the aqueous phase was then adjusted to ca. 4, using 1M HCl. The aqueous layer was then extracted three times with additional DCM. The organic layers were pooled, dried over sodium sulfate, filtered and then concentrated to obtain 3.59 g of 2-(4-bromophenyl)-2-methylpropanoic acid, as a white solid, which gave LC/MS and proton NMR spectra consistent with theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919343B2
Source datasetuspto-grants-2005_07
ORD IDord-42b0688ed54f445696fa4fb32e2ef1b7
Source noteuspto-grants-2005_07