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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 551375Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/551375

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
Edukt2-BromothiopheneHCID 13851—
EduktAmmonium ChlorideHCID 25517—
EduktMagnesiumHCID 5462224—
EduktOxo-thiophen-2-yl-acetic acid 1-methyl-piperidin-4-ylmethyl esterHCID 67197151—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHydroxy-di-thiophen-2-yl-acetic acid 1-methyl-piperidin-4-ylmethyl esterHCID 67198340—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07947730B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-2dc5cd17fa8442369188dfb862bef6cc
Quellennotizuspto-grants-2011_05