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HRID 340478作成日:2026年10月25日

Iodine → 2-Chloro-5-fluoro-4-iodopyridine

https://huagongshe.com/reaction/340478

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Sodium ThiosulfateHCID 24477—
反応物2-Chloro-5-fluoropyridineHCID 2782801—
反応物Lithium di-isopropylamideHCID 86591433—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Oxolane--water (1/1)HCID 21881883—
生成物2-Chloro-5-fluoro-4-iodopyridineHCID 2482049546.7%

反応条件

温度-75 °C

反応手順

A tetrahydrofuran (5 ml) solution containing 2-chloro-5-fluoropyridine (500 mg) was added to a tetrahydrofuran (20 ml) solution containing lithium-N,N-diisopropylamide (2M tetrahydrofuran/ethylbenzene/heptane solution) (2.9 ml) at −75° C. in a nitrogen atmosphere, followed by stirring at −75° C. for 3 hours. Subsequently, a tetrahydrofuran (5 ml) solution containing iodine (1.16 g) was added, followed by stirring at −75° C. for 1 hour. Then, water/tetrahydrofuran (2 ml/8 ml), water (10 ml), and 3M aqueous sodium thiosulfate were slowly added at −75° C., −50° C., and −35° C., respectively, to the reaction solution. The reaction solution was adjusted to room temperature, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=20:1 to 10:1), and a white solid of 2-chloro-5-fluoro-4-iodopyridine (457 mg) was thus obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895585B2
出典データセットuspto-grants-2014_11
ORD IDord-b1df6db62d3646958c54f88f02cbc85c
出典メモuspto-grants-2014_11