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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 256413Erstellt: 24. Oktober 2026

Pyridine → 1-(Benzyloxy)-2-(chloromethyl)benzene

https://huagongshe.com/de/reaction/256413

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktSalicyl AlcoholHCID 5146—
EduktBenzyl ChlorideHCID 7503—
EduktBenzenemethanol, 2-(phenylmethoxy)-HCID 18811—
EduktThionyl ChlorideHCID 24386—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelEthanolHCID 702—
LösungsmittelChloroformHCID 6212—
Produkt1-(Benzyloxy)-2-(chloromethyl)benzeneHCID 56350781%

Reaktionsschritte

To a solution of 46.5 (0.217 mole) 2-benzyloxybenzyl alcohol (prepared by reaction of 2-hydroxybenzyl alcohol with benzyl chloride in ethanol containing an equimolar amount of potassium t-butoxide at 100° C.) in 100 ml chloroform was added 17.2 g (0.217 mole) pyridine followed by dropwise addition of a solution of 25.8 g (0.217 mole) thionyl chloride in 60 ml chloroform. The resulting mixture was heated at reflux for 1.5 hours, cooled, washed with water, brine and dried (MgSO4). Evaporation of solvent gave 45.8 g crude oil which was distilled in vacuo to yield 40.7 g (81%) of product as a colorless oil, b.p. 141° C.(1 Torr).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04703052
Quelldatensatzuspto-grants-1987_10
ORD IDord-e57e3edb022740a8926893137e99290e
Quellennotizuspto-grants-1987_10