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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607754Generated: October 30, 2026

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

https://huagongshe.com/reaction/1607754

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866206
Source datasetuspto-grants-1989_09
ORD IDord-10b47b92bf4148578689f32ad145f79c
Source noteuspto-grants-1989_09