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HRID 885834作成日:2026年10月27日

Potassium Hydroxide → (E)-3-(4-{(E)-3-[4-(1-methyl-piperidin-4-yl)-phenyl]-3-oxo-propenyl}-phenyl)-acrylic acid tert-butyl ester

https://huagongshe.com/reaction/885834

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物4-Formylcinnamic acid tert-butyl esterHCID 54147604—
反応物1-(4-(1-Methylpiperidin-4-yl)phenyl)ethan-1-one hydrochlorideHCID 67049733—
溶媒EthanolHCID 702—
生成物(E)-3-(4-{(E)-3-[4-(1-methyl-piperidin-4-yl)-phenyl]-3-oxo-propenyl}-phenyl)-acrylic acid tert-butyl esterHCID 6704948629.1%

反応手順

A mixture of 1-[4-(1-methyl-piperidin-4-yl)-phenyl]-ethanone hydrochloride (544 mg, 2.15 mmol), 4-formylcinnamic acid tert-butyl ester (500 mg, 2.15 mmol) and 1.7 M KOH (3.8 ml, 6.46 mmol) in EtOH (10 ml) was stirred at room temperature for 6 hours. During the reaction, the formation of a precipitate was observed. The solid was then filtered off through a Buchner funnel to obtain 270 mg of (E)-3-(4-{(E)-3-[4-(1-methyl-piperidin-4-yl)-phenyl]-3-oxo-propenyl}-phenyl)-acrylic acid tert-butyl ester as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08242175B2
出典データセットuspto-grants-2012_08
ORD IDord-2125cb7bae3943d9bbf74a534e66d532
出典メモuspto-grants-2012_08