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HRID 714189作成日:2026年10月25日

Acetone → 4-[3-Methoxy-4-(methoxymethoxy)phenyl]but-3-en-2-one

https://huagongshe.com/reaction/714189

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-Methoxy-4-(methoxymethoxy)benzaldehydeHCID 79661—
溶媒EthanolHCID 702—
生成物4-[3-Methoxy-4-(methoxymethoxy)phenyl]but-3-en-2-oneHCID 6950168297.7%

反応手順

4-Methoxymethyloxy-3-methoxybenzaldehyde (1j, 2.30 g, 11.7 mmol) and acetone (19, 8.75 ml, 118.4 mmol) were combined in ethanol (20 ml) and stirred for 15 min at room temperature. A solution of sodium hydroxide (0.80 g, 20.0 mmol) and water (20 ml) was added and the mixture stirred for 1 hr at room temperature. The resulting mixture was extracted into ethyl acetate, washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to afford a solid. The crude solid was recrystallized from hexane to give 2.70 g (97%) of a white solid: mp 73-75° C.; 1H NMR: δ 2.34 (s, 3H), 3.48 (s, 3H), 3.89 (s, 3H), 5.24 (s, 2H), 6.58 (d, 1H, J=16.1 Hz), 7.07 (m, 2H), 7.13 (d, 1H, J=8.7 Hz), 7.43 (d, 1H, J=16.1 Hz); 13C NMR: δ 27.4, 55.9, 56.3, 95.2, 110.4, 115.9, 122.5, 125.7, 128.7, 143.1, 148.7, 149.8, 198.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187397B2
出典データセットuspto-grants-2015_11
ORD IDord-738f3df2774248cd809c7e3afb861164
出典メモuspto-grants-2015_11