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HRID 1913486作成日:2026年10月25日

Ethyl 2-pyridinecarboxylate → 1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-3-(pyridin-2-yl)propane-1,3-dione

https://huagongshe.com/reaction/1913486

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-pyridinecarboxylateHCID 17307—
反応物Sodium hydrideHCID 24758—
反応物1,4-Benzodioxan-6-yl methyl ketoneHCID 76143—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-3-(pyridin-2-yl)propane-1,3-dioneHCID 5684038471%

反応手順

A solution of 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)ethanone (XV) (1 eq) in THF was added slowly to a suspension of NaH (1.5 eq) in THF stirred under nitrogen at room temperature. The solution was further allowed to stir at room temperature until the evolution of gas was ceased. Ethyl picolinate (XIX) (1.1 eq) was added to the solution and refluxed overnight under nitrogen. The solution was cooled, poured into ice water and extracted with ethyl acetate. The organic layer was dried over MgSO4, filtered and concentrated under vacuum. The crude product was purified by column chromatography over silica gel to produce 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-(pyridin-2-yl)propane-1,3-dione 15 as a yellow solid (71% yield), 1H NMR (CDCl3, 400 MHz): δ ppm 4.13-4.43 (m, 4H), 6.94 (d, J=8.31 Hz, 1H), 7.42 (m, 1H), 7.44 (m, 1H) 7.59 (m, 2H), 7.85 (m, 1H), 8.14 (d, J=7.81, 1H), 8.65 (m, 1H); ESIMS found C16H13NO4 m/z 284 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08609717B2
出典データセットuspto-grants-2013_12
ORD IDord-e8711200dcac40fb83074b6114e73e66
出典メモuspto-grants-2013_12