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HRID 1244144作成日:2026年10月27日

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

https://huagongshe.com/reaction/1244144

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物1-(4-Methyl-2-thienyl)ethan-1-oneHCID 83654—
反応物BistrifluoroacetoxyiodobenzeneHCID 12041285—
溶媒Carbon TetrachlorideHCID 5943—
溶媒DichloromethaneHCID 6344—
生成物1-(5-Iodo-4-methyl-thiophen-2-yl)-ethanoneHCID 2193154566.2%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07119205B2
出典データセットuspto-grants-2006_10
ORD IDord-dc3083b835fa49c48a6b93a87bff5204
出典メモuspto-grants-2006_10