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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487207Generated: October 31, 2026

N-bromobutanimide → Methyl 2-(bromomethyl)-4-nitrobenzoate

https://huagongshe.com/reaction/1487207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-methyl-4-nitrobenzoateHCID 15088700—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 2-(bromomethyl)-4-nitrobenzoateHCID 15088701—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-methyl-4-nitrobenzoic acid methyl ester (696 mg, 3.57 mmol), azobisisbutyronitrile (58.6 mg, 0.357 mmol) and N-bromosuccinimide (785 mg, 4.46 mmol) were suspended in carbon tetrachloride (35 mL) in a sealed tube. The above mixture was flushed with nitrogen for 5 minutes and heated at 80° C. for 22 hours. After cooling, the solid was filtered off and the filtrate was concentrated to dryness to obtain the crude product methyl 2-(bromomethyl)-4-nitrobenzoate as a light-brown solid, which was used for the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428508B2
Source datasetuspto-grants-2016_08
ORD IDord-c34485451b3f434b867472e16d7846d4
Source noteuspto-grants-2016_08