関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl Malonate | HCID 7761 | — |
| 反応物 | Ethanol sodium ethoxide | HCID 23706232 | — |
| 反応物 | 1-Tert-butoxycarbonylpiperidine-4-ylbenzenesulfonate | HCID 86615851 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07557112B2 |
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| 出典データセット | uspto-grants-2009_07 |
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| ORD ID | ord-83d2f5a5043c4c058f48fc3d80f22423 |
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| 出典メモ | uspto-grants-2009_07 |
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