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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678709Generated: October 25, 2026

N-bromobutanimide → 1-(Bromomethyl)-4-methoxy-2-nitrobenzene

https://huagongshe.com/reaction/1678709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-Methyl-3-nitroanisoleHCID 87137—
SolventCarbon TetrachlorideHCID 5943—
Product1-(Bromomethyl)-4-methoxy-2-nitrobenzeneHCID 3747830—

Reaction Steps

4-Methyl-3-nitroanisole (2.7 mL; manufactured by Sigma-Aldrich Co.) was dissolved in carbon tetrachloride (20 mL; manufactured by Wako Pure Chemical Industries, Ltd.), and NBS (4.0520 g; manufactured by Tokyo Chemical Industry Co., Ltd.) and hydrated benzoyl peroxide (348 mg; manufactured by Sigma-Aldrich Co.) were added to the solution. The mixture was purged with nitrogen, and was stirred for 3 hours at reflux. The reaction solution was filtered, and then the filtrate was washed with an aqueous solution of NaHSO3 and water and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by column chromatography (“COLUMN-B”; n-hexane:ethyl acetate=94:6→73:27). Thus, the title compound (3.2549 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008506B2
Source datasetuspto-grants-2011_08
ORD IDord-160003e9764547afa9c7eb3bf7cabab0
Source noteuspto-grants-2011_08