戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 350051作成日:2026年10月27日

Water → Ethyl 3-[1-[4-(2-methyl-3-pyridylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]propionate

https://huagongshe.com/reaction/350051

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物3-(Chloromethyl)-2-methylpyridineHCID 12243711—
反応物Ethyl 3-[1-(4-hydroxybenzyl)-4-phenyl-3-pyrrolyl]propionateHCID 23024736—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 3-[1-[4-(2-methyl-3-pyridylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]propionateHCID 6942388885.4%

反応手順

Sodium hydride (60%, oily, 60.0 mg) was added to a solution of ethyl 3-[1-(4-hydroxybenzyl)-4-phenyl-3-pyrrolyl]propionate (524 mg) in N,N-dimethylformamide (10 ml) at 0° C., and the mixture was stirred at room temperature for 15 minutes. 3-Chloromethyl-2-methylpyridine (212 mg) was added to the mixture, which was stirred at room temperature for 15 minutes. The reaction mixture was poured into water, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), then concentrated. The residue was subjected to silica gel column chromatography, and ethyl 3-[1-[4-(2-methyl-3-pyridylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]propionate (581 mg, yield: 85%) was obtained as an oily substance from the fraction eluted with ethyl acetate-hexane (1:1, volume ratio).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07179823B1
出典データセットuspto-grants-2007_02
ORD IDord-e7e5105838014747855bc85c6d101c87
出典メモuspto-grants-2007_02