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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091041Generated: October 31, 2026

Azobisisobutyronitrile → HCID 66778012, compound

https://huagongshe.com/reaction/2091041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 16433918HCID 16433918—
SolventAcetonitrileHCID 6342—
ProductHCID 66778012HCID 6677801271.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution (150 mL) of methyl 5-fluoro-3-methyl-1-benzofuran-2-carboxylate (15.4 g) synthesized above in acetonitrile were added N-bromosuccinimide (19.8 g) and 2,2′-azobis(isobutyronitrile) (1.21 g), and the mixture was stirred under argon atmosphere at 50° C. for 2.5 days. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (20-30% ethyl acetate/hexane) to give a white solid. The obtained solid was washed with hexane to give the title object compound (15.1 g, 71%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-7dd68d411ba64cd4a507be06ffe86142
Source noteuspto-grants-2013_05