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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1612753Erstellt: 27. Oktober 2026

Benzyl Bromide → 3-(Phenylmethyl)-2-piperidinone

https://huagongshe.com/reaction/1612753

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
Edukt2-PiperidoneHCID 12665—
EduktAmmonium ChlorideHCID 25517—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(Phenylmethyl)-2-piperidinoneHCID 443899553,9%

Reaktionsbedingungen

Temperatur-40 °C

Reaktionsschritte

To a stirred solution of 2-piperidone (40 g, 0.404 mol) in tetrahydrofuran (800 ml) at 0° C. was added, over a period of 2 hours, n-butyl lithium (2.5 M in hexane, 356 ml, 0.889 mol). The reaction was cooled to -40° C. and a solution of benzyl bromide (48 ml, 0.404 mol) in tetrahydrofuran (200 ml) was added dropwise over a period of 2 hours. The reaction was allowed to warm slowly to room temperature and stirred for 12 hours. Water (100 ml) and saturated aqueous ammonium chloride (100 ml) were added and the aqueous phase separated and extracted with ethyl acetate (3×100 ml). The combined organic phases were washed with brine (200 ml), dried with sodium sulphate and evaporated in vacuo. The resulting solid was recrystallised from toluene to give the desired product as white needles (41.2 g), m.pt. 120°-123° C. Low resolution mass spectroscopy revealed the mass/charge ratio of the parent molecule ion, M+, to be 190 thereby confirming the molecular of the product to be 190.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05190958
Quelldatensatzuspto-grants-1993_03
ORD IDord-cd7327f7984e4c9994003e601f8a031c
Quellennotizuspto-grants-1993_03