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HRID 77658作成日:2026年10月23日

Acetone → 1,5-Bis(2-trifluoromethylphenyl)-1,4-pentadien-3-one

https://huagongshe.com/ja/reaction/77658

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o-(Trifluoromethyl)benzaldehydeHCID 123067—
溶媒EthanolHCID 702—
生成物1,5-Bis(2-trifluoromethylphenyl)-1,4-pentadien-3-oneHCID 8543407988.7%

反応手順

2-(Trifluoromethyl)-benzaldehyde (1w, 0.75 ml, 5.7 mmol) and acetone (19, 0.21 ml, 2.8 mmol) were combined in ethanol (20 ml) and stirred for 10 min at room temperature. A solution of sodium hydroxide (0.34 g, 8.5 mmol) and water (15 ml) was added and the mixture stirred for 18 hr at room temperature. The resulting precipitate was filtered and recrystallized from ethanol to afford 0.92 g (87%) of a yellow solid: mp 131-133° C. [expected mp 131° C.]; 1H NMR: δ 6.99 (d, 2H, J=15.9 Hz), 7.48 (t, 2H, J=7.6 Hz), 7.56 (t, 2H, J=7.0 Hz), 7.70 (d, 2H, J=7.7 Hz), 7.77 (d, 2H, J=7.6 Hz), 8.07 (d, 2H, J=15.7 Hz); 13C NMR: δ 123.9, 126.2, 127.9, 128.8, 129.4, 129.7, 132.1, 133.7, 139.1, 188.0.

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-c9985af20dab4ee99bc1dd8b010eb9cc
出典メモuspto-grants-2014_09