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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951601Generated: October 27, 2026

Hydrogen Bromide → Methyl 3-(4-acetyl-2-methylphenyl)-2-bromopropionate

https://huagongshe.com/reaction/1951601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantMethyl AcrylateHCID 7294—
Reactant1-(4-Amino-3-methylphenyl)ethanoneHCID 13355515—
ReactantSodium NitriteHCID 23668193—
CatalystHCID 178419072HCID 178419072—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl 3-(4-acetyl-2-methylphenyl)-2-bromopropionateHCID 8663668982%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(4-Amino-3-methylphenyl)ethanone (1.70 g, 11.39 mmol) was dissolved in methanol (15 mL)-acetone (38 mL). The solution was cooled to 0° C. 48% Hydrobromic acid (5.15 mL, 45.56 mmol) was dropwise added to the solution for 1 minute. A solution of sodium nitrite (943 mg, 13.67 mmol) in water (1.8 mL) was further added to the solution. The mixture was stirred at the same temperature for 30 minutes. The mixture was left to room temperature. Methyl acrylate (7.23 mL, 80.30 mmol) and copper(I) oxide (117 mg) were added to the mixture. The resulting mixture was stirred at 40° C. for 30 minutes. The solvent was removed under reduced pressure. Ice-cold water (150 mL) was added to the residue. The mixture was neutralized with ammonia water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried with anhydrous sodium sulfate. The solvent was removed under reduced pressure to give the desired compound (2.79 g) as brown oil (yield 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404726B2
Source datasetuspto-grants-2013_03
ORD IDord-79f2029a133e40f5bf088a6ec8631bd9
Source noteuspto-grants-2013_03