Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 575527Erstellt: 25. Oktober 2026

Hexane → tert-Butyl 4-(2-((methanesulfonyl)oxy)ethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/575527

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktEthyl AcetateHCID 8857—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 854140—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-Butyl 4-(2-((methanesulfonyl)oxy)ethyl)piperidine-1-carboxylateHCID 1522959691%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Combine tert-butyl 4-(2-hydroxyethyl)piperidine-1-carboxylate (4.720 kg, 20.6 mol) with DCM (40 L) and TEA (3020 mL, 21.63 mol) in a 50 L reactor under a nitrogen atmosphere. Cool the solution to about 0° C. and slowly add methane sulfonyl chloride (2.478 kg, 21.63 mol) in DCM (5 L) while keeping the reaction temperature below 10° C. After the addition is complete stir the mixture for 18 h at 15° C. at which time TLC (1:1, hexane:EtOAc) shows no starting material remaining Wash the mixture with water (30 L) and allow the phases to separate. Concentrate the organic phase to a solid. Slurry the solid in MTBE (6 L), collect by filtration, and dry in a vacuum oven at 50° C. to provide the title compound as a white solid (5.67 kg, 91%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09035051B1
Quelldatensatzuspto-grants-2015_05
ORD IDord-cb238508ccae4c429e4b2be14587a653
Quellennotizuspto-grants-2015_05