Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995563Generated: October 30, 2026

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

https://huagongshe.com/reaction/1995563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant3-Chloro-1-propanolHCID 12313—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product((3-Chloropropoxy)methyl)benzeneHCID 22150597.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

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 1 N 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 the title compound, (108.4 g), bp0.01 60°-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04405530
Source datasetuspto-grants-1983_09
ORD IDord-9cf304bf4b37432080c170b1179ab472
Source noteuspto-grants-1983_09