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HRID 25783作成日:2026年10月25日

Water → 4-{1-[((E)-but-2-enyl)oxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/25783

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-Butene, 1-bromo-HCID 122414—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
反応物4-(1-hydroxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 20760332—
溶媒Dimethyl SulfoxideHCID 679—
生成物4-{1-[((E)-but-2-enyl)oxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 2076033173.2%

反応手順

A mixture of 70 mg of 4-(1-hydroxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl ester in 2 mL of DMSO was treated with 0.22 mL of 1.0 M sodium bis(trimethylsilyl)amide and 29 mg of crotyl bromide at room temperature. The reaction mixture was allowed to stir at room temperature overnight. The reaction was worked up by adding water and extracted with EtOAc three times. The organic layers were combined, washed sequentially with saturated aqueous sodium bicarbonate solution, water, and brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash chromatography to yield 58 mg of 4-{1-[((E)-but-2-enyl)oxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl ester as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858627B2
出典データセットuspto-grants-2005_02
ORD IDord-98eef52007ea4f0caa6af926eb09b25a
出典メモuspto-grants-2005_02