戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 554312作成日:2026年10月25日

Sodium Carbonate → 4-Methyl-5-phenyl-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/554312

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物Sodium HydroxideHCID 14798—
反応物Phenylboronic AcidHCID 66827—
反応物5-bromo-4-methyl-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 86232734—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物4-Methyl-5-phenyl-1H-pyrrole-3-carbaldehydeHCID 7136281281.1%

反応条件

温度100 °C

反応手順

A suspension of 5-bromo-4-methyl-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde (1.78 g), phenylboronic acid (1.37 g), dichloro[bis(triphenylphosphine)]palladium (0.19 g) and sodium carbonate (1.72 g) in 1,2-dimethoxyethane (30 mL)-water (10 mL) was stirred at 100° C. for 1 hr. 8 mol/L aqueous sodium hydroxide solution (15 mL) was added, and the mixture was stirred at 90° C. for 3 hr. After cooling, the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→1:1), and the obtained solid was washed with hexane to give the title compound as a pale-yellow solid (yield 815 mg, 69%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08048909B2
出典データセットuspto-grants-2011_11
ORD IDord-a74a70bfe43a4cb2931cf901d08132ae
出典メモuspto-grants-2011_11