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HRID 911312作成日:2026年10月25日

Triethylamine → 2-Cyano-3-fluoropyridine

https://huagongshe.com/reaction/911312

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Trimethylsilyl cyanideHCID 82115—
反応物Pyridine, 3-fluoro-, 1-oxideHCID 123084—
溶媒AcetonitrileHCID 6342—
生成物2-Cyano-3-fluoropyridineHCID 706040870.3%

反応手順

Dissolve 3-fluoropyridine-N-oxide (1.0 g, 8.687 mmol) in anhydrous acetonitrile (100 mL). Add triethylamine (1.319 g, 1.82 mL, 13.031 mmol), trimethylsilylcyanide (3.447 g, 4.63 mL, 34.749 mmol) and heat the mixture to reflux overnight. Cool to ambient temperature and concentrate in vacuo. Dissolve the residue in EtOAc and wash with saturated aqueous NaHCO3. Dry the organic layer over Na2SO4, filter, and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane/EtOAc (1:0 and 17:3) to give the desired intermediate as a solid (746 mg, 70%). GC-MS m/z: 122 (M+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08022062B2
出典データセットuspto-grants-2011_09
ORD IDord-3dd873d0c5e14629b3ff0b6ae470974e
出典メモuspto-grants-2011_09