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HRID 844869作成日:2026年10月26日

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

https://huagongshe.com/reaction/844869

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Trifluoroacetic anhydrideHCID 9845—
反応物N-IodosuccinimideHCID 120273—
反応物1,3-Dimethyl-6-(trifluoromethyl)uracilHCID 2758669—
反応物sodium thiosulfite anhydrousHCID 15847209—
溶媒Potassium CarbonateHCID 11430—
生成物1,3-Dimethyl-5-iodo-6-(trifluoromethyl)uracilHCID 2261371466%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06380387B1
出典データセットuspto-grants-2002_04
ORD IDord-93837f21262b4ec49dfe9dd9dc9a902d
出典メモuspto-grants-2002_04