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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586758Generated: November 2, 2026

Azobisisobutyronitrile → Methyl 3-(bromomethyl)-2-nitrobenzoate

https://huagongshe.com/reaction/1586758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantBenzoic acid, 3-methyl-2-nitro-, methyl esterHCID 79621—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 3-(bromomethyl)-2-nitrobenzoateHCID 22509333—

Reaction Steps

Methyl 2-nitro-3-methylbenzoate (15.3 gm) was suspended in carbon tetrachloride (45 mL) along with N-bromosuccinimide (15 3 gm) and heated to reflux. 2,2'-Azobis(2-methylpropionitrile) (AIBN) (0.4 gm) was added to the refluxing solution in four equal portions over 48 hours. The reaction was cooled to room temperature, filtered, and concentrated. The residue consisted of a mixture of starting material, desired product, and dibrominated material which were difficult to separate and so were used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05216003
Source datasetuspto-grants-1993_06
ORD IDord-b826b036ebb145d39ce59f71411d453c
Source noteuspto-grants-1993_06