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HRID 2225517作成日:2026年10月27日

Sodium Chloride → 1-(4-Hydroxy-3-methoxycinnamoyl)-4-methylpiperidine-4-carboxylic acid

https://huagongshe.com/reaction/2225517

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物Ammonium formateHCID 2723923—
反応物Allyl 1-(4-allyloxy-3-methoxycinnamoyl)-4-methylpiperidine-4-carboxylateHCID 53899198—
触媒HCID 178418476HCID 178418476—
溶媒TetrahydrofuranHCID 8028—
生成物1-(4-Hydroxy-3-methoxycinnamoyl)-4-methylpiperidine-4-carboxylic acidHCID 53657751125.1%

反応手順

0.4 g of bis(triphenylphosphine)palladium dichloride and 5 g of ammonium formate were added to a solution of 1.1 g of allyl 1-(4-allyloxy-3-methoxycinnamoyl)-4-methylpiperidine-4-carboxylate (Example 67) in 100 ml of THF. Under an argon stream, the solution was reacted for hours, while it was refluxed. After reaction, 150 ml of an aqueous sodium chloride solution was added to the reaction solution. The solution was extracted three times with 50 ml of ethyl acetate. The organic layer obtained was washed three times with an aqueous sodium chloride solution and dried over magnesium sulfate. Thereafter, the solvent was removed in vacuo, yielding 1.1 g of 1-(4-hydroxy-3-methoxycinnamoyl)-4-methylpiperidine-4-carboxylic acid (a compound of the present invention) as a pale yellow oil, which had the following physiochemical properties:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05344845
出典データセットuspto-grants-1994_09
ORD IDord-e22296aa17354f3abaa1c0380a77b429
出典メモuspto-grants-1994_09