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HRID 550789作成日:2026年10月27日

Toluene → Tert-butyl 4-(1,3-dihydroxypropan-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/550789

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Lithium borohydrideHCID 4148881—
反応物Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonateHCID 59605280—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 4-(1,3-dihydroxypropan-2-yl)piperidine-1-carboxylateHCID 59605609—

反応手順

A mixture of 1-tert-butoxycarbonylpiperidin-4-ol, triethylamine, benzenesulfonyl chloride, and methylene chloride was stirred at ambient temperature for 2 days to yield 1-tert-butoxycarbonylpiperidin-4-yl benzenesulfonate. A mixture of 1-tert-butoxycarbonylpiperidin-4-yl benzenesulfonate obtained, diethyl malonate, 20% NaOEt-EtOH, and EtOH was heated under reflux with stirring for 22 hours to yield diethyl[1-(tert-butoxycarbonyl)piperidin-4-yl]malonate. A mixture of diethyl [1-(tert-butoxycarbonyl)piperidin-4-yl]malonate obtained, lithium borohydride, toluene, and THF was stirred at 60° C. for 18 hours to yield 2-(1-tert-butoxycarbonylpiperidin-4-yl)propane-1,3-diol, which was stirred together with 4M HCl-dioxane solution in MeOH at ambient temperature for 1 hour to yield 2-piperidin-4-ylpropane-1,3-diol hydrochloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947690B2
出典データセットuspto-grants-2011_05
ORD IDord-87ede17518a846378837ace766085197
出典メモuspto-grants-2011_05