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HRID 77656作成日:2026年10月23日

Acetone → 1,5-Bis(3-fluorophenyl)-1,4-pentadien-3-one

https://huagongshe.com/ja/reaction/77656

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物WaterHCID 962—
反応物Sodium HydroxideHCID 14798—
反応物3-FluorobenzaldehydeHCID 68009—
溶媒EthanolHCID 702—
生成物1,5-Bis(3-fluorophenyl)-1,4-pentadien-3-oneHCID 6950172242%

反応手順

3-Fluorobenzaldehyde (1s, 0.5 ml, 4.7 mmol) and acetone (19, 0.18 ml, 2.3 mmol) were combined in ethanol (20 ml) and stirred for 10 min at room temperature. A solution of sodium hydroxide (0.29 g, 7.3 mmol) and water (15 ml) was added and the mixture stirred for 18 hr at room temperature. The resulting mixture was filtered and chromatographed on silica gel with ethyl acetate/hexane to give a solid. The crude was recrystallized from ethanol to afford 0.26 g (42%) of yellow crystals: mp 96-97° C. [expected mp 96-97° C.]; 1H NMR: δ 7.03 (d, 2H, J=16.1 Hz), 7.09 (m, 2H), 7.35 (m, 6H), 7.67 (d, 2H, J=15.9 Hz); 13C NMR: δ 114.4, 117.5, 124.4, 126.3, 130.4, 136.9, 142.0, 162.9, 188.1; Anal. Calcd for C17H12OF2: C, 75.55; H, 4.48. Found: C, 75.26; H, 4.65.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841326B2
出典データセットuspto-grants-2014_09
ORD IDord-b896188ea0824f719c74a4f42878ee58
出典メモuspto-grants-2014_09