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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107475Generated: October 30, 2026

Methane → 3-(4-Bromophenyl)-2-methylpropanoic acid

https://huagongshe.com/reaction/1107475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantDiethyl 2-(4-bromobenzyl)-2-methylmalonateHCID 21186275—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product3-(4-Bromophenyl)-2-methylpropanoic acidHCID 2171419188%

Reaction Conditions

Temperature205 °C

Reaction Steps

A solution of sodium hydroxide (34.0 g) in water (155 ml) was added to a solution of diethyl 2-(4-bromobenzyl)-2-methylmalonate (29.2 g) in ethanol (165 ml), and then heated under reflux for 9 hours. The reaction mixture was cooled, the solvent was evaporated and the residue taken up in water (150 ml). Sodium hydroxide pellets were added (25.4 g) and the reaction mixture was heated under reflux for 2 hours. The reaction mixture was then cooled and acidified to pH<1 with concentrated hydrochloric acid, which caused precipitation of a solid. The reaction mixture was extracted with diethyl ether (3×150 ml), the combined organic layers were dried (MgSO4) and then the solvent was evaporated to give a white solid. This solid was heated at 205° C. for 20 minutes, cooled to ambient temperature, dissolved in 1.0 M sodium hydroxide solution (150 ml), treated with activated charcoal and then filtered through diatomaceous earth. The resulting clear solution was re-acidified and then extracted with diethyl ether (3×150 ml). The combined organic layers were dried (MgSO4) and evaporated to give a yellow oil which crystallised on standing to give 2-methyl-3-(4-bromophenyl)propanoic acid as a white solid (18.2 g), m.p. 69-70° C.; mass spectrum (+ve CI): 243 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060475
Source datasetuspto-grants-2000_05
ORD IDord-4d64422910c94be7949957d287e137f4
Source noteuspto-grants-2000_05