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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1244144Erstellt: 26. Oktober 2026

Iodine → 1-(5-Iodo-4-methyl-thiophen-2-yl)-ethanone

https://huagongshe.com/reaction/1244144

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
Edukt1-(4-Methyl-2-thienyl)ethan-1-oneHCID 83654—
EduktBistrifluoroacetoxyiodobenzeneHCID 12041285—
LösungsmittelCarbon TetrachlorideHCID 5943—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(5-Iodo-4-methyl-thiophen-2-yl)-ethanoneHCID 2193154566,2%

Reaktionsschritte

Commercially available 1-(4-Methyl-thiophen-2-yl)-ethanone (2.0 g, 14.2 mmol) was combined with bis(trifluoroacetoxy)iodobenzene (6.3 g, 14.2 mmol) and iodine (3.6 g, 14.2 mmol) in CCl4 (30 ml). The purple suspension was stirred for 2 h upon which time the reaction was judged to be complete by HPLC. The reaction was diluted with CH2Cl2 and washed with Na2S2O3 (aq, sat.) until the purple color dissipated. The organics were washed with H2O and brine. The aqueous layers were extracted once with CH2Cl2 and the combined organics were dried (Na2SO4), filtered and concentrated by rotary evaporation to give a yellow residue which was purified by flash column chromatography (hexanes:ethyl acetate gradient 2–50% ethyl acetate) to give 1-(5-Iodo-4-methyl-thiophen-2-yl)-ethanone (2.5 g, 66%) as a solid; MS (ESI) m/z 266.9 (M+H+); 1H NMR (300 MHz, DMSO-d6) δ 7.65 (s, 1H), 2.47 (s, 3H), 2.19 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07119205B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-dc3083b835fa49c48a6b93a87bff5204
Quellennotizuspto-grants-2006_10