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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206822Generated: October 27, 2026

N-bromobutanimide → 1,3-Dibromo-2,4-dimethoxybenzene

https://huagongshe.com/reaction/2206822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-1,3-dimethoxybenzeneHCID 612296—
SolventAcetonitrileHCID 6342—
Product1,3-Dibromo-2,4-dimethoxybenzeneHCID 1164505395.1%

Reaction Steps

17.9 g of 1-bromo-2,6-dimethoxybenzene and 200 mL of acetonitrile were placed in a flask, and the resulting mixture was cooled on ice. Then, 14.7 g of N-bromosuccinimide was added. Then, while heating the reaction solution to room temperature, stirring was conducted for 8 hours. 2.39 g of N-bromosuccinimide was further added, and stirring was conducted at room temperature for 7 hours. After completion of the stirring, the solvent was distilled off under reduced pressure. Residues were dissolved in dichloromethane, and washed sequentially with sodium thiosulfate and saturated saline. An organic phase was dried with magnesium sulfate and concentrated. Residues were purified by means of silica gel column chromatography, whereby 23.2 g (yield: 95%) of colorless oil of 1,3-bromo-2,6-dimethoxybenzene was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09373792B2
Source datasetuspto-grants-2016_06
ORD IDord-30dc6c2b67c34d17b24c05766107cebb
Source noteuspto-grants-2016_06