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HRID 225471作成日:2026年10月25日

Diethyl Malonate → Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonate

https://huagongshe.com/reaction/225471

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl MalonateHCID 7761—
反応物Ethanol sodium ethoxideHCID 23706232—
反応物1-Tert-butoxycarbonylpiperidine-4-ylbenzenesulfonateHCID 86615851—
溶媒EthanolHCID 702—
生成物Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonateHCID 59605280—

反応手順

A mixture of 1-tert-butoxycarbonylpiperidine-4-ol, triethylamine, benzenesulfonyl chloride and methylene chloride was stirred for two days at room temperature to give 1-tert-butoxycarbonylpiperidine-4-ylbenzenesulfonate. A mixture of the obtained 1-tert-butoxycarbonylpiperidine-4-ylbenzenesulfonate, diethyl malonate, 20% sodium ethoxide-EtOH solution and EtOH was stirred for 22 hours heated to reflux to give diethyl[1-(tert-butoxycarbonyl)piperidine-4-yl]malonate. A mixture of the obtained diethyl[1-(tert-butoxycarbonyl)piperidine-4-yl]malonate, lithium borohydride, toluene and THF was stirred for 18 hours at 60° C. to give 2-(1-tert-butoxycarbonylpiperidine-4-yl)propane-1,3-diol. A mixture of the obtained 2-(1-tert-butoxycarbonylpiperidine-4-yl)propane-1,3-diol, 4M HCl-dioxane solution and MeOH was stirred for one hour at room temperature to give 2-piperidine-4-ylpropane-1,3-diol hydrochloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557112B2
出典データセットuspto-grants-2009_07
ORD IDord-83d2f5a5043c4c058f48fc3d80f22423
出典メモuspto-grants-2009_07