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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 379933Erstellt: 25. Oktober 2026

1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine → tert-Butyl 4-(acetylthio)piperidine-1-carboxylate

https://huagongshe.com/reaction/379933

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
EduktPotassium ethanethioateHCID 23670855—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkttert-Butyl 4-(acetylthio)piperidine-1-carboxylateHCID 22494773905,4%

Reaktionsbedingungen

Temperatur105 °C

Reaktionsschritte

In 40 ml of dimethylformamide were dissolved 4.12 g (14.7 mmol) of 1-(tert-butoxycarbonyl)-4-(methanesulfonyloxy)piperidine, and 2.53 g (2.21 mmol) of potassium thioacetate were added to the solution, followed by stirring of the resulting mixture at 105° C. for 4 hours under nitrogen atmosphere. After cooling, the reaction mixture was diluted with ethyl acetate and washed with water and then a saturated aqueous NaCl solution, followed by evaporation of the solvent. The thus obtained residue was subjected to silica gel column chromatography and the fractions eluted with a mixed solvent of hexane-ethyl acetate (5:1) were collected to obtain 5.19 g (yield: 81%) of the title compound as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06300357B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-bffff60e8d2d40cca11441a4679f6732
Quellennotizuspto-grants-2001_10