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HRID 552277作成日:2026年10月26日

5-Ethyl-4-phenyl-thiophene-2-carboxylic acid → 1-(5-Ethyl-4-phenyl-thiophen-2-yl)-ethanone

https://huagongshe.com/reaction/552277

反応式

関与物質

役割名称HCID仕込み量
反応物5-Ethyl-4-phenyl-thiophene-2-carboxylic acidHCID 67166421—
反応物HCID 178418348HCID 178418348—
溶媒TetrahydrofuranHCID 8028—
生成物1-(5-Ethyl-4-phenyl-thiophen-2-yl)-ethanoneHCID 67166164—

反応手順

At 5° C. a solution of 5-ethyl-4-phenyl-thiophene-2-carboxylic acid (180 mg, 0.775 mmol) in THF (4 mL) is treated with MeLi (0.9 mL, 1.6 M in diethyl ether). The reaction mixture is stirred at rt for 30 min before another portion of MeLi (0.5 mL) is added. Stirring is continued for 1 h, the reaction is quenched by adding water (50 mL) and extracted with EA. The organic extract is dried over MgSO4, the solvent is removed in vacuo, and the crude product is purified by CC on silica gel eluting with heptane:EA 30:1 to give 1-(5-ethyl-4-phenyl-thiophen-2-yl)-ethanone (64 mg) as a colourless oil; LC-MS: tR=1.03 min, [M+1+MeCN]+=272.15; 1H NMR (CDCl3): δ 7.60 (s, 1H), 7.47-7.32 (m, 5H), 2.91 (q, J=7.6 Hz, 2H), 2.54 (s, 3H), 1.30 (t, J=7.6 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07951794B2
出典データセットuspto-grants-2011_05
ORD IDord-105c59f248dc4ed9bae4ef820754fe68
出典メモuspto-grants-2011_05