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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308414Generated: November 2, 2026

1,6-Dibromohexane → 1-[4-[(6-Bromohexyl)oxy]butyl]benzene

https://huagongshe.com/reaction/2308414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,6-DibromohexaneHCID 12368—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzenebutanolHCID 76889—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventTolueneHCID 1140—
Product1-[4-[(6-Bromohexyl)oxy]butyl]benzeneHCID 11012439—

Reaction Steps

A mixture of 10 ml (0.0655 mol) of 4-phenylbutanol and 20 ml of toluene is added within 15 minutes, with stirring, to a mixture of 20.2 ml (0.131 mol) of 1,6-dibromohexane, 16 g of powdered (0.242 mol KOH) caustic potash, 2.2 g (0.0066 mol) tetra-n-butylammonium hydrogen sulphate and 50 ml of toluene, at a temperature between 25 and 30° C. After it has all been added the mixture is rinsed with 5 ml of toluene and stirred for 2 hours at a temperature between 25 and 30° C. Then 75 ml of water are added, the organic phase is separated off and washed twice with 50 ml of water. The organic phase is concentrated under reduced pressure using the rotary evaporator and the residue is fractionally distilled under a high vacuum (p<0.1 mbar). 14.62 g (71% of theory) of the title compound are obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06835857B2
Source datasetuspto-grants-2004_12
ORD IDord-2cab214b76df4fab9cc4189f68396c83
Source noteuspto-grants-2004_12