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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2367895Erstellt: 26. Oktober 2026

Sodium Hydroxide → 1-Dimethylamino-4-hydroxy-piperidine-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/2367895

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktPotassium BicarbonateHCID 516893—
Edukt1-Dimethylamino-4-hydroxy-piperidine-4-carbonitrileHCID 86671308—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelMethanolHCID 887—
Produkt1-Dimethylamino-4-hydroxy-piperidine-4-carboxylic acid methyl esterHCID 67225501—

Reaktionsschritte

4.2 g 1-Dimethylamino-4-hydroxy-piperidine-4-carbonitrile is dissolved in 30 ml of a hydrochloric acid solution in methanol (10% HCl in methanol) and the reaction mixture is stirred at room temperature for 2 days. After 24 hours, the reaction vessel is saturated with hydrochloric acid gas. To bring the reaction to completion, the mixture is diluted with 100 ml methanol, saturated with hydrochloric acid gas and further stirred at room temperature overnight, then neutralized under cooling by addition of 40 ml NaOH 30% (to pH 6) and a saturated aqueous potassium bicarbonate solution (to pH 8). The solution is concentrated, the residue partitioned between ethyl acetate and water, the water layer extracted with ethyl acetate, the combined organic layer dried over sodium sulfate, and the solvent evaporated. The residue is purified by chromatography on silica gel, with ethyl acetate/methanol/triethylamine as a solvent (gradient 95/2.5/2.5 to 90/5/5). Thus, 2.27 g 1-Dimethylamino-4-hydroxy-piperidine-4-carboxylic acid methyl ester is obtained. 1H-NMR (CDCl3): 3.78 ppm (s, 3H), 2.90 ppm (s, broad, 1H), 2.82 ppm (m, 2H), 2.70 ppm (m, 2H), 2.41 ppm (s, 6H), 2.11 ppm (m, 2H), 1.69 ppm (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08703165B2
Quelldatensatzuspto-grants-2014_04
ORD IDord-e40e551756bc4b35897904169c563fb1
Quellennotizuspto-grants-2014_04