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HRID 897471作成日:2026年10月26日

Water → 2-(4-Iodophenoxy)pyrimidine

https://huagongshe.com/reaction/897471

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物N-IodosuccinimideHCID 120273—
反応物2-PhenoxypyrimidineHCID 5324768—
溶媒Trifluoroacetic acidHCID 6422—
溶媒Trifluoroacetic anhydrideHCID 9845—
生成物2-(4-Iodophenoxy)pyrimidineHCID 148461750%

反応手順

A mixture of 2-phenoxypyrimidine (int AY) (4.03 g, 0.0234 mol) and N-iodosuccinimide (10.52 g, 0.0468 mol) in trifluoroacetic acid (40 mL) and trifluoroacetic anhydride (8 mL) was heated at reflux for 4 hours. The mixture was allowed to cool to ambient temperature and water (75 mL) was added. The mixture was extracted with three times with 50 mL. The combined organic layers were washed twice with saturated aqueous sodium bicarbonate (50 mL), twice with 10% aqueous sodium thiosulfate (50 mL) and brine (50 mL). The organic layer was dried over magnesium sulfate, filtered and the solvent was removed in vacuo. The crude solid was purified by flash column chromatography on silica gel using n-heptane/ethyl acetate (3:1) as an eluent to give 2-(4-iodophenoxy)pyrimidine as a light yellow solid (3.49 g, 0.0117 mol): 1H NMR (CDCl3, 400 MHz) 8.57 (d, 2H), 7.73 (d, 2H), 7.07 (t, 1H), 6.98 (d 2H); TLC (n-heptane/ethyl acetate=1:1) Rf 0.45.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06921763B2
出典データセットuspto-grants-2005_07
ORD IDord-d901760092454903a32d8b8b602290fa
出典メモuspto-grants-2005_07