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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 642909Erstellt: 24. Oktober 2026

p-Toluenesulfonic acid → 4-(1-Benzylpiperidin-4-yl)morpholine

https://huagongshe.com/de/reaction/642909

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktMorpholineHCID 8083—
EduktPotassium CarbonateHCID 11430—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt1-Benzyl-2-piperidoneHCID 5170076—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(1-Benzylpiperidin-4-yl)morpholineHCID 783831—

Reaktionsschritte

30 mL (0.162 Mol) 1-benzylpiperidone (L) and 16.1 mL (0.185 Mol) morpholine (M) are dissolved in 407 mL tetrahydrofuran at ambient temperature. While cooling, 1.0 g (5 mmol) of p-toluenesulphonic acid and 14.6 mL glacial acetic acid are added, whereupon a jelly-like precipitate is formed. 52.19 g (0.246 Mol) sodium triacetoxyborohydride are added while cooling with ice, during which time the reaction temperature rises to 30° C. After 4 hours at 20° C., 90 mL water are added dropwise. After another 30 minutes, 280 mL of 17% potassium carbonate solution are added. The mixture is stirred intensively, while gas is observed to be given off. After separation of the phases the organic phase is dried and evaporated down. Yield: 33.0 g (78% of theory)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07696346B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-b152b6f43a19429a8b1b02915dbfe146
Quellennotizuspto-grants-2010_04