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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 552277Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/552277

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Ethyl-4-phenyl-thiophene-2-carboxylic acidHCID 67166421—
EduktHCID 178418348HCID 178418348—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(5-Ethyl-4-phenyl-thiophen-2-yl)-ethanoneHCID 67166164—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07951794B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-105c59f248dc4ed9bae4ef820754fe68
Quellennotizuspto-grants-2011_05