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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417757Generated: October 29, 2026

Dimethylformamide → 6-(4-Vinylbenzyloxy)bromohexane

https://huagongshe.com/reaction/417757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium hydrideHCID 24758—
Reactant(4-Vinylphenyl)methanolHCID 2735162—
SolventWaterHCID 962—
Product6-(4-Vinylbenzyloxy)bromohexaneHCID 5786453358%

Reaction Steps

A DMF suspension (5 ml) of sodium hydride (50% in oil, 240 mg, 5.0 mmoles) was cooled to 0° C. under an argon atmosphere, and a DMF (1 ml) solution of 1.34 g of 4-vinylbenzyl alcohol (10 mmoles) was added. The reaction mixture was agitated for fifteen minutes, and a DMF solution (3 ml) of 3.66 g of 1,6-dibromohexane (15 mmoles) was added over at least five minutes. The reaction mixture was agitated at room temperature for three hours. Fifteen milliliters of water was added to the reaction solution while cooling using ice, and the solution was agitated for five minutes. The solution was extracted using ethyl acetate (2×40 ml). The combined organic layers were washed using 15 ml of saturated aqueous saline solution and dried using anhydrous sodium sulfate. Upon filtration and concentration, 4.11 g of the residue was purified using silica gel column chromatography (70 g silica gel, 20:1 hexane/Et2O) and 1.72 g of 6-(4-vinylbenzyloxy)bromohexane (5.8 mmoles, 58%) was obtained in the form of an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08092720B2
Source datasetuspto-grants-2012_01
ORD IDord-6809c694e9f747359c1544392d1414b4
Source noteuspto-grants-2012_01