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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1252565Erstellt: 25. Oktober 2026

Benzyl Bromide → ((3-Chloropropoxy)methyl)benzene

https://huagongshe.com/reaction/1252565

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
Edukt3-Chloro-1-propanolHCID 12313—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt((3-Chloropropoxy)methyl)benzeneHCID 22150597,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

In a 2 l flask, a mixture of 3-chloropropanol (56.7 g), benzyl bromide (102.6 g) and dry THF (600 ml) is stirred and cooled with ice/salt mixture. Potassium tert-butoxide (70 g) is added in portions (5-10 g), maintaining the internal temperature at about 0° C. After the mixture is stirred for 3 more hours at room temperature, the solvent is evaporated. Addition of 1N HCl (1 l), extraction with ether (1 l), and evaporation of solvent gives crude material (113.6 g), which is distilled under vacuum to give 1-chloro-3-benzyloxypropane (108.4 g) b.p.0.01 60°-80° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04743691
Quelldatensatzuspto-grants-1988_05
ORD IDord-b483449bc0fd4f7599dd80dfb18cf900
Quellennotizuspto-grants-1988_05