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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 398025Erstellt: 24. Oktober 2026

Benzyl Bromide → 4-Benzyloxyphenylacetonitrile

https://huagongshe.com/de/reaction/398025

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Edukt4-Hydroxybenzyl cyanideHCID 26548—
LösungsmittelAcetoneHCID 180—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-BenzyloxyphenylacetonitrileHCID 522804358,3%

Reaktionsschritte

4-Hydroxybenzyl cyanide (2.5 g, 18.77 mmol), benzyl bromide (3.8 g, 22:5 mmol) and potassium carbonate (45 mmol) were combined in acetone (50 mL) and heated to reflux for 8 h. The reaction was allowed to cool to rt, diluted with ethyl acetate and filtered to remove the solids. The organic layer was concentrated in vacuo to give an oil. The crude benzyl ether was purified by chromatography on silica gel eluting hexane:ethyl acetate (90:10, v:v) to give 4-benzyloxybenzyl cyanide (4.0 g, 95%) which solidified. MS (M+NH4)+=241.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06610731B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-bc2d91ce438746bbbad4db8247c636a0
Quellennotizuspto-grants-2003_08