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HRID 225472Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/225472

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktLithium borohydrideHCID 4148881—
EduktDiethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonateHCID 59605280—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 4-(1,3-dihydroxypropan-2-yl)piperidine-1-carboxylateHCID 59605609—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07557112B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-26f0533af1dd422bbc294f5456e4851a
Quellennotizuspto-grants-2009_07