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HRID 2216727作成日:2026年10月27日

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

https://huagongshe.com/reaction/2216727

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-bromopropionateHCID 79040—
反応物4-Methyl-5-phenylthiophene-2-carbaldehydeHCID 12323253—
触媒ZincHCID 23994—
触媒Mercury dibromideHCID 24612—
溶媒BenzeneHCID 241—
溶媒WaterHCID 962—
生成物2-Methyl-3-(4-methyl-5-phenyl-2-thienyl)-acrylic acidHCID 67174636—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07112638B2
出典データセットuspto-grants-2006_09
ORD IDord-b0e976d4de05414aae0e9b66c3180f7c
出典メモuspto-grants-2006_09