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HRID 38631作成日:2026年10月26日

Acetovanillone → 2',3'-Dihydroxyacetophenone

https://huagongshe.com/reaction/38631

反応式

関与物質

役割名称HCID仕込み量
反応物AcetovanilloneHCID 2214—
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
溶媒AcetonitrileHCID 6342—
生成物2',3'-DihydroxyacetophenoneHCID 642911070.3%

反応条件

温度25 °C

反応手順

To a solution of acetovanillone (33) (4.70 g, 28.3 mmol) in MeCN (60 mL) was added K2CO3 (8.05 g, 58.3 mmol) and KI (0.20 g, 1.2 mmol). The mixture was stirred under N2 atmosphere and benzyl bromide (34) (4.0 mL, 34 mmol) was added dropwise. The reaction mixture was reflux for 24 h and then cooled to 25° C., then resulting precipitate was filtered off. The filtrate was evaporated and purified by column chromatography (SiO2, n-hexane: CH2Cl2=1:2) to give 30. White solid; yield: 70.3%; mp 87-88° C.; 1H-NMR (CDCl3. 200 MHz): δ 2.51 (s, 3H), 3.91 (s, 3H), 5.20 (s, 2H), 6.86 (d, J=8.2 Hz, 1H), 7.21-7.55 (m, 7H); 13C-NMR (CDCl3, 50 MHz): δ 26.19, 56.05, 70.79, 110.53, 112.13, 123.07, 127.18, 128.10, 128.68, 130.72, 136.28, 149.49, 152.41, 196.80; Anal. calcd for C16H16O3: C, 74.98; H, 6.29. Found: C, 75.02; H, 6.25.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524740B2
出典データセットuspto-grants-2013_09
ORD IDord-904a19f9ad764a429ae73edd9fd181c0
出典メモuspto-grants-2013_09