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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 844869생성일: 2026년 10월 25일

Trifluoroacetic acid → 1,3-Dimethyl-5-iodo-6-(trifluoromethyl)uracil

https://huagongshe.com/reaction/844869

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Trifluoroacetic anhydrideHCID 9845—
반응물N-IodosuccinimideHCID 120273—
반응물1,3-Dimethyl-6-(trifluoromethyl)uracilHCID 2758669—
반응물sodium thiosulfite anhydrousHCID 15847209—
용매Potassium CarbonateHCID 11430—
생성물1,3-Dimethyl-5-iodo-6-(trifluoromethyl)uracilHCID 2261371466%

반응 단계

A mixture of 1,3-dimethyl-6-(trifluoromethyl)uracil (16.91 mmol, 3.52 g), trifluoroacetic acid (20 mL) and trifluoroacetic anhydride (5 mL) was refluxed for 5 min. Then, NIS (16.91 mmol, 3.8 g) was added and the resulting mixture was stirred for 15 h at which time the TLC analysis of the reaction mixture indicated the presence of some starting material. Another portion of NIS (8.45 mmol, 1.9 g) was added and reflux was continued for another 5 h. The reaction mixture was cooled to room temperature and was poured slowly into a saturated potassium carbonate solution (100 mL). Then, sodium thiosulfite solution was added to remove the excess iodine color. The resulting solids were collected by filtration and washed with water. After air drying, 3.73 g (66% yield) of 1,3-dimethyl-5-iodo-6-(trifluoromethyl)uracil was obtained as a white solid: mp 149-151° C. EI-HRMS m/e calcd for C7H6F3IN2O2 (M+) 333.9426, found 333.9436.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06380387B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-93837f21262b4ec49dfe9dd9dc9a902d
출처 메모uspto-grants-2002_04