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HRID 7161作成日:2026年10月23日

Dimethylformamide → 2-Fluoropyridine-3-carbaldehyde

https://huagongshe.com/ja/reaction/7161

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物2-FluoropyridineHCID 9746—
反応物Ammonium ChlorideHCID 25517—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2-Fluoropyridine-3-carbaldehydeHCID 1143494415%

反応条件

温度-78 °C

反応手順

A solution of 2-fluoropyridine (306 mg, 3.15 mmol) in THF (1 mL) was added to a solution of lithium diisopropylamide in THF (0.20 M, 17 mL, 3.4 mmol) at −78° C. The solution was stirred at −78° C. for 4 h, then DMF (0.73 mL, 9.4 mmol) was added dropwise and stirring was continued at −78° C. for 2.5 h. Saturated NH4Cl(aq) (2 mL) was added, and the mixture was allowed to warm to room temperature. The mixture was diluted with EtOAc (20 mL), and the organic phase was washed with saturated NaHCO3(aq) (20 mL) and brine (10 mL), then dried (MgSO4) and concentrated in vacuo. Purification of the crude material by chromatography on silica gel (10% EtOAc/hexanes) gave the title compound as a yellow liquid (58 mg, 15%). 1H NMR (CDCl3) □ 7.39 (m, 1H), 8.32 (m, 1H), 8.48 (m, 1H), 10.33 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084155B2
出典データセットuspto-grants-2006_08
ORD IDord-ae7961b104604450beaed78f4ad54709
出典メモuspto-grants-2006_08