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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216727Generated: October 26, 2026

Ethyl 2-bromopropionate → 2-Methyl-3-(4-methyl-5-phenyl-2-thienyl)-acrylic acid

https://huagongshe.com/reaction/2216727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-bromopropionateHCID 79040—
Reactant4-Methyl-5-phenylthiophene-2-carbaldehydeHCID 12323253—
CatalystZincHCID 23994—
CatalystMercury dibromideHCID 24612—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product2-Methyl-3-(4-methyl-5-phenyl-2-thienyl)-acrylic acidHCID 67174636—

Reaction Steps

A mixture of 2-formyl-4-methyl-5-phenylthiophene (20.2 g, 0.1 mol) and ethyl-2-bromopropionate (0.12 mol, 15.5 mL) was added to a suspension of Zn (7 g, 0.1 mol) in 150 mL of benzene with a catalytic amount of HgBr2. The resulting mixture was refluxed under stirring while all amount of Zn will not be dissolved, and subsequently dissolved in water. The organic layer was isolated, washed with a 10% aq. solution of HCl, dried over MgSO4 and evaporated off to dryness. The residue, corresponding to 2-methyl-3-(4-methyl-5-phenyl-2-thienyl)ethyl acrylate, was used without further purification in the synthesis of the related acid. In fact, it was added to a 30% aq. solution of sodium hydroxide in 100 mL of ethanol and refluxed for 2 h. The resulting reaction mixture was diluted in water, acidified and filtered. The precipitate was dried under P2O5. Yield 16.7 g (65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112638B2
Source datasetuspto-grants-2006_09
ORD IDord-b0e976d4de05414aae0e9b66c3180f7c
Source noteuspto-grants-2006_09