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HRID 1711220作成日:2026年10月25日

Potassium ethoxide → 3-(2-Nitro-3-piperidin-1-yl-phenyl)-2,5-dioxo-hexanedioic acid di ethyl ester

https://huagongshe.com/reaction/1711220

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium ethoxideHCID 23670592—
反応物3-(2-Nitro-3-piperidin-1-yl-phenyl)-2-oxo-propionic acid ethyl esterHCID 59796771—
反応物Bromoethyl pyruvateHCID 86587973—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2-Nitro-3-piperidin-1-yl-phenyl)-2,5-dioxo-hexanedioic acid di ethyl esterHCID 59796786—

反応手順

A solution of 3-(2-nitro-3-piperidin-1-yl-phenyl)-2-oxo-propionic acid ethyl ester (ii) in THF is treated with potassium ethoxide (“KOEt”) (1 eq), followed by bromoethyl pyruvate (1.05 eq), at 0° C. The reaction is allowed to warm to room temperature over 90 min. The reaction is diluted with water and ether, partitioned, and the aqueous layer is washed with ether. The combined organic layers are dried over MgSO4, filtered and concentrated. Chromatography gives 3-(2-nitro-3-piperidin-1-yl-phenyl)-2,5-dioxo-hexanedioic acid diethyl ester (iii).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07790724B2
出典データセットuspto-grants-2010_09
ORD IDord-7a09d29648ba441496f25efeae018233
出典メモuspto-grants-2010_09