戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 922173作成日:2026年10月26日

Potassium Carbonate → Methyl 3-{4-[(3-benzoylbenzyl)oxy]phenyl}propanoate

https://huagongshe.com/reaction/922173

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Benzenepropanoic acid, 4-hydroxy-, methyl esterHCID 79706—
反応物3-(Bromomethyl)benzophenoneHCID 89586—
溶媒DimethylformamideHCID 6228—
生成物Methyl 3-{4-[(3-benzoylbenzyl)oxy]phenyl}propanoateHCID 6668558683.3%

反応手順

To a 250 mL RB flask fitted with magnetic stirrer was charged 45 mL of DMF. To the stirred solvent was added 3-(4-Hydroxy-phenyl)-propanoic acid methyl ester (4.5 g, 16.35 mmol) followed by K2CO3 (6.78 g, 49.074 mmol) and the resulting mixture stirred at room temperature for 30 minutes. (3-bromomethyl-phenyl)-phenyl-methanone (2.94 g, 16.35 mmol) was added to the above mixture and stirring continued at RT for 24 h. After completion of the reaction (reaction monitored by TLC), reaction solvent was removed under reduced pressure. The crude compound was purified by column chromatography on silica gel (100/200 mesh) using petroleum ether (60-80) and ethyl acetate as eluent which yielded the product as yellow color oil (5.1 g, Yield: 83.3%): MS (ESI, 120 eV): m/z=375.1 (M+H)+; 1H NMR (300 MHz, CDCl3): δ 7.68 (s, 1H), 7.62-7.66 (d, 3H), 7.57-7.59 (d, 1H), 7.53 (m, 1H), 7.45-7.50 (m, 3H), 7.11-7.13 (d, 2H), 6.88-6.90 (d, 2H), 5.10 (s, 2H), 3.66 (s, 3H), 2.85-2.92 (m, 2H), 2.56-2.62 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09278915B2
出典データセットuspto-grants-2016_03
ORD IDord-ef92470ef89f417582c29d0fbf27735f
出典メモuspto-grants-2016_03