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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2216727Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2216727

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 2-bromopropionateHCID 79040—
Edukt4-Methyl-5-phenylthiophene-2-carbaldehydeHCID 12323253—
KatalysatorZincHCID 23994—
KatalysatorMercury dibromideHCID 24612—
LösungsmittelBenzeneHCID 241—
LösungsmittelWaterHCID 962—
Produkt2-Methyl-3-(4-methyl-5-phenyl-2-thienyl)-acrylic acidHCID 67174636—

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07112638B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-b0e976d4de05414aae0e9b66c3180f7c
Quellennotizuspto-grants-2006_09