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HRID 551375作成日:2026年10月27日

Iodine → Hydroxy-di-thiophen-2-yl-acetic acid 1-methyl-piperidin-4-ylmethyl ester

https://huagongshe.com/reaction/551375

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物2-BromothiopheneHCID 13851—
反応物Ammonium ChlorideHCID 25517—
反応物MagnesiumHCID 5462224—
反応物Oxo-thiophen-2-yl-acetic acid 1-methyl-piperidin-4-ylmethyl esterHCID 67197151—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Hydroxy-di-thiophen-2-yl-acetic acid 1-methyl-piperidin-4-ylmethyl esterHCID 67198340—

反応手順

A solution of 2-bromothiophene (2.15 ml, 22.2 mmol) in THF (15 ml) is added dropwise to a mixture of magnesium (0.54 g, 22.2 mmol) and a single crystal of iodine in THF (15 ml). After addition of just under one half of the 2-bromothiophene the addition is suspended until reaction has initiated (judged by an exotherm). The addition is then completed maintaining the reaction temperature to below 40° C. After the addition is completed the reaction mixture is heated to reflux for 20 minutes. This mixture is then cooled and added to a solution of oxo-thiophen-2-yl-acetic acid 1-methyl-piperidin-4-ylmethyl ester (4.6 g, 17.2 mmol) in THF (40 ml). After the addition is completed the reaction mixture is stirred at room temperature for 1 hour and then heated to reflux for 2.5 hours. After cooling to room temperature saturated aqueous ammonium chloride solution (100 ml) is added together with diethylether. The solution is extracted with diethylether dried over magnesium sulphate, filtered and concentrated. Purification by flash silica column chromatography gives the title product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947730B2
出典データセットuspto-grants-2011_05
ORD IDord-2dc5cd17fa8442369188dfb862bef6cc
出典メモuspto-grants-2011_05