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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385945Generated: October 31, 2026

Azobisisobutyronitrile → HCID 15457079, compound

https://huagongshe.com/reaction/1385945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 15457083HCID 15457083—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 15457079HCID 1545707979%

Reaction Steps

0.98 g (2.72 mmol) of 3-(7-chloro-5-fluoro-2-methylbenzofuran-4-yl)-1-methyl-6-trifluoromethyl-2-(1H)-pyridone was dissolved in 25 ml of carbon tetrachloride, and 0.51 g (2.86 mmol) of NBS and 0.04 g (0.27 mmol) of 2,2′-azobisisobutyronitrile were added thereto, followed by refluxing for 2 hours. Succinic acid imide was removed by filtration. Then, carbon tetrachloride was distilled off under reduced pressure, and the obtained residue was poured into water and extracted with ethyl acetate. After washing with water, the organic layer was dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off under reduced pressure, and the obtained crude crystals were washed with n-hexane to obtain 0.94 g (yield: 79%) of the desired product. Melting point: 142-144° C. 1H-NMR (300 MHz, CDCl3) δ value: 3.73(3H,s), 4.56(2H,s), 6.66(1H,s), 6.80(1H,d), 7.20(1H,d), 7.55(1H,d)ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265349B1
Source datasetuspto-grants-2001_07
ORD IDord-6fc4bdbe5ac9490693b744e57027f24b
Source noteuspto-grants-2001_07