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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1401976Erstellt: 24. Oktober 2026

Sodium Sulfate → Tert-butyl 4-(5-chloro-2-methoxyphenyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/de/reaction/1401976

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium SulfateHCID 24436—
EduktSodium BisulfateHCID 516919—
Edukt2-Bromo-4-chloroanisoleHCID 521935—
Edukttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktTert-butyl 4-(5-chloro-2-methoxyphenyl)-4-hydroxypiperidine-1-carboxylateHCID 5877248039%

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

To a stirred solution of 2-bromo-4-chloroanisole (164 g, 0.74 mol) in tetrahydrofuran (1 L), cooled at −70° C. and under an atmosphere of argon, was added butyl lithium (2.7 M in heptane, 280 ml) over a period of 1 hour. The mixture was stirred for 30 minutes, maintaining the temperature at −70° C., before the addition of N-boc-4-piperidone (145 g, 0.73 mol) in tetrahydrofuran (250 ml) over a period of 1 hour. The reaction temperature was warmed to −40° C. over 2 hours before the addition of sodium hydrogen sulphate (5M aqueous, 160 ml), sodium sulphate (300 g) and hexane (500 ml). The mixture was stirred for 10 hours. The organic layer was decanted, filtered through silica gel (300 g, 63/100 μm) washing with ethyl acetate:hexane (4:6, by volume, 2×400 ml). The filtrate was evaporated in vacuo and the residue recrystallized from ethyl acetate:hexane to afford the title compound as white crystals, 100 g, 39% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08907101B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-b547530a686e4e11ad75cb3f5b5eb618
Quellennotizuspto-grants-2014_12