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HRID 40248作成日:2026年10月24日

N-Fluorobenzenesulfonimide → Methyl 2-fluoro-2-(quinolin-6-yl)acetate

https://huagongshe.com/ja/reaction/40248

反応式

関与物質

役割名称HCID仕込み量
反応物N-FluorobenzenesulfonimideHCID 588007—
反応物Methyl 6-quinolineacetateHCID 1514202—
反応物Lithium HexamethyldisilazideHCID 2733832—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-fluoro-2-(quinolin-6-yl)acetateHCID 57691374—

反応条件

温度-78 °C

反応手順

To a 250 ml round-bottomed flask was added lithium bis(trimethylsilyl)amide (2.0 g, 12 mmol) and tetrahydrofuran (75 ml). The mixture was cooled to −78° C. and methyl 2-(quinolin-6-yl)acetate (2.0 g, 9.9 mmol) was added as a solution in 1 ml THF. After stirring at −78° C. for 30 min, n-fluorobenzenesulfonimide (3.8 g, 12 mmol) was added as a 1 M solution in THF. This was stirred for 30 min at −78° C. and then allowed to warm to rt. The mixture was quenched with sat NH4Cl (50 mL) and diluted with water (200 mL). The mixture was concentrated in vacuo to remove the THF and then was extracted with EtOAc (2×100 ml). The combined extracts were washed with brine (100 ml), dried (Na2SO4) and concentrated onto silica. Purification by silica gel chromatography (20 to 60% EtOAc/hexane) afforded the title compound as a tan solid. MS (ESI, pos. ion) m/z: 220 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524900B2
出典データセットuspto-grants-2013_09
ORD IDord-8e6617c9f4714da98aa60cb1ba84aabd
出典メモuspto-grants-2013_09