돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1244144생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1244144

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물1-(4-Methyl-2-thienyl)ethan-1-oneHCID 83654—
반응물BistrifluoroacetoxyiodobenzeneHCID 12041285—
용매Carbon TetrachlorideHCID 5943—
용매DichloromethaneHCID 6344—
생성물1-(5-Iodo-4-methyl-thiophen-2-yl)-ethanoneHCID 2193154566.2%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07119205B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-dc3083b835fa49c48a6b93a87bff5204
출처 메모uspto-grants-2006_10