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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 551375생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/551375

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물2-BromothiopheneHCID 13851—
반응물Ammonium ChlorideHCID 25517—
반응물MagnesiumHCID 5462224—
반응물Oxo-thiophen-2-yl-acetic acid 1-methyl-piperidin-4-ylmethyl esterHCID 67197151—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물Hydroxy-di-thiophen-2-yl-acetic acid 1-methyl-piperidin-4-ylmethyl esterHCID 67198340—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947730B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-2dc5cd17fa8442369188dfb862bef6cc
출처 메모uspto-grants-2011_05