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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078084Generated: November 1, 2026

Azobisisobutyronitrile → HCID 15672392, compound

https://huagongshe.com/reaction/1078084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2,3-Pyridinedicarboxylic acid, 5-methyl-, 2,3-dimethyl esterHCID 11745869—
ReactantHCID 15672391HCID 15672391—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 15672392HCID 1567239257%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of dimethyl 5-methyl-2,3-pyridinedicarboxylate (30.0 g, 0.143 mol), N-bromosuccinimide (32.0 g, 0.18 mol) and 2,2'-azobisisobutyronitrile (0.9 g, 0.0055 mol) in carbon tetrachloride (200 mL) is heated at 80° C. for 1.5 hours. Additional 2,2'-azobisisobutyronitrile (0.9 g, 0.0055 mol) is added and the reaction mixture is heated at reflux for 2 hours, cooled to room temperature and filtered. The filter cake is washed with carbon tetrachloride. The filtrate and wash are combined, washed with water and concentrated in vacuo to give an oil. The oil is shown by HPLC to contain 57% of the title product, 16% dimethyl 5-methyl-2,3-pyridinedicarboxylate and 23% dimethyl 5-dibromomethyl-2,3-pyridinedicarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545835
Source datasetuspto-grants-1996_08
ORD IDord-2c40abd583c94340885c2e4fe10ad240
Source noteuspto-grants-1996_08