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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814729Generated: October 30, 2026

1,4-Benzodioxan → 6-Bromo-1,4-benzodioxane

https://huagongshe.com/reaction/1814729

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-BenzodioxanHCID 10301—
ReactantN-bromobutanimideHCID 67184—
SolventDimethylformamideHCID 6228—
Product6-Bromo-1,4-benzodioxaneHCID 104141—

Reaction Steps

35 g of 1,4-benzodioxane and 200 ml of anhydrous dimethylformamide are placed under argon at 0° C. 54.9 g of N-bromosuccinimide are then added in portions. After it has returned gradually to room temperature, the reaction mixture is stirred for 24 hours. The solvents are evaporated off under reduced pressure and the white solid obtained is washed with dichloromethane. The filtrate is treated with 50 ml of saturated aqueous sodium sulfate solution, washed with 50 ml of saturated aqueous sodium chloride solution and dried over magnesium sulfate. After evaporation of the solvents under reduced pressure, a yellow oil is obtained (quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878665B2
Source datasetuspto-grants-2005_04
ORD IDord-5a63ab5bb6204fe0aacb73c0310cd7a0
Source noteuspto-grants-2005_04