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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473481Generated: October 26, 2026

Azobisisobutyronitrile → Methyl 2-(bromomethyl)-4-nitrobenzoate

https://huagongshe.com/reaction/473481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantSuccinimideHCID 11439—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-methyl-4-nitrobenzoateHCID 15088700—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 2-(bromomethyl)-4-nitrobenzoateHCID 15088701—

Reaction Steps

In accordance with general method T, 4.70 g (24.00 mmol) of (1) are dissolved in 30 ml of carbon tetrachloride, with heating, and 5.00 g (28.00 mmol) of N-bromosuccinimide and 2 spatula tips of azobisisobutyronitrile are then added. The mixture is refluxed for 6 h with irradiation with a 500 W spotlight. On cooling to room temperature, succinimide separates out, and is filtered off. The filtrate is evaporated on a rotary evaporator in order to obtain the product as a yellow oil. Yield: 5.85 g (88.8%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633312B2
Source datasetuspto-grants-2014_01
ORD IDord-803e764bf1dd4180ac70060ea340f3a1
Source noteuspto-grants-2014_01