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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199137Generated: October 29, 2026

Azobisisobutyronitrile → Methyl 3,5-dibromo-4-(bromomethyl)benzoate

https://huagongshe.com/reaction/2199137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMethyl 3,5-dibromo-4-methylbenzoateHCID 624016—
ReactantN-BromosuccinamideHCID 9834204—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 3,5-dibromo-4-(bromomethyl)benzoateHCID 2264794899%

Reaction Steps

A solution of methyl 3,5-dibromo-4-methylbenzoate (5 g, 16.24 mmol) in carbon tetrachloride (50 mL) was treated with N-bromosuccinamide (3.6 g, 20.23 mmol) and 2,2′-azobisisobutyronitrile (0.56 g, 3.410 mmol). The reaction mixture was heated to reflux for 24 h. The reaction was cooled to room temperature and concentrated under vacuum. The resulting mixture was absorbed onto silica and was purified by flash chromatography using silica gel eluted with 3:1 hexanes: ethyl acetate. The desired fractions were collected and concentrated under vacuum to afford a solid which was dried under high vacuum to afford 3,5-dibromo-4-bromomethyl-benzoic acid methyl ester (57) (6.22 g, 99%) as a yellow solid; LRMS for C9H7Br3O2 (M+Na) m/z=407. MW=386.8669, Exact Mass=383.7996

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE046024E1
Source datasetuspto-grants-2016_06
ORD IDord-9d3a7b7891234c4baba24d02a9b46b6e
Source noteuspto-grants-2016_06