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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404357Generated: November 1, 2026

Azobisisobutyronitrile → HCID 66677503, compound

https://huagongshe.com/reaction/2404357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantPotassium CarbonateHCID 11430—
ReactantN-bromobutanimideHCID 67184—
ReactantSarcosine t-butyl ester hydrochlorideHCID 11252350—
Reactant3,5-Difluoro-4-methylbenzonitrileHCID 45073538—
SolventAcetonitrileHCID 6342—
ProductHCID 66677503HCID 66677503—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a degassed solution of 3,5-difluoro-4-methylbenzonitrile (1.53 g, 10 mmol) and AIBN (0.033 g; 0.20 mmol) in ACN (40 mL) was added N-bromo-succinimide (2.14 g, 12.0 mmol). The reaction mixture was heated at 90° C. for 24 hours. The solvent was evaporated in vacuo and the residue partitioned between water and DCM. The organic phase was passed through a hydrophobic frit and the solvent evaporated in vacuo. The residue was dissolved in CAN, and then sarcosine t-butyl ester hydrochloride (1.09 g, 6.0 mmol) and K2CO3 (2.07 g, 15 mmol) added. The reaction mixture was stirred at 70° C. for 18 hours. The suspension was filtered and the filtrate evaporated in vacuo. The residue was purified by flash chromatography (silica, iso-hexane/EtOAc) to afford the title compound. 1H NMR (CDCl3, 400 MHz) δ 7.22 (2H, d, J=5.9 Hz), 3.94 (2H, s), 3.21 (2H, s), 2.41 (3H, s), 1.48 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802704B2
Source datasetuspto-grants-2014_08
ORD IDord-07cf41eaf9d5453aba025d06bba2fc77
Source noteuspto-grants-2014_08