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HRID 513658作成日:2026年10月25日

8-Nitro-7-quinolinecarboxaldehyde → (3-Fluoro-phenyl)-(8-nitro-quinolin-7-yl)-methanol

https://huagongshe.com/reaction/513658

反応式

関与物質

役割名称HCID仕込み量
反応物8-Nitro-7-quinolinecarboxaldehydeHCID 11769554—
反応物HCID 178505773HCID 178505773—
溶媒TetrahydrofuranHCID 8028—
生成物(3-Fluoro-phenyl)-(8-nitro-quinolin-7-yl)-methanolHCID 6818344158.1%

反応条件

温度-78 °C

反応手順

3-Fluorophenyl magnesium bromide (1 M solution in THF; 0.86 ml, 4.33 mmol) was added dropwise to a solution of 8-nitroquinoline-7-carbaldehyde (Intermediate 204) (0.35 g, 1.73 mmol) in dry THF (5 ml) at −78° C. and the mixture was stirred at −78° C. for 1 h. The reaction was quenched with saturated NH4Cl solution and the aqueous phase was extracted with EtOAc. The organic phase was washed with brine, dried (Na2SO4) and concentrated in vacuo. The crude residue was purified by column chromatography with DCM as the eluent to give the title compound (0.3 g, 58%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09102688B2
出典データセットuspto-grants-2015_08
ORD IDord-fe13ca0ea02f414ab50d65eaf24e1a38
出典メモuspto-grants-2015_08