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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230014Generated: October 31, 2026

Azobisisobutyronitrile → Methyl 3-bromo-4-(bromomethyl)benzoate

https://huagongshe.com/reaction/230014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 3-bromo-4-methylbenzoateHCID 7015747—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 3-bromo-4-(bromomethyl)benzoateHCID 10804694—

Reaction Steps

To a solution of 1.09 g (4.76 mmol) of the product from Example 224 Step A in 7 mL of carbon tetrachloride was added 847 mg (4.76 mmol) of N-bromosuccinimide and 78 mg (0.48 mmol) of 2,2′-azobisisobutyronitrile. The resultant mixture was heated at reflux for 2 5 hours, cooled to ambient temperature, diluted with carbon tetrachloride and filtered through celite. The filtrate was concentrated in vacuo and carried on without purification assuming 100% conversion. HPLC/MS (ESI) m/z (M+H)=310.9 (3.68 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563815B2
Source datasetuspto-grants-2009_07
ORD IDord-9718766ead334480b6cec93aef000a77
Source noteuspto-grants-2009_07