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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404353Generated: November 3, 2026

Azobisisobutyronitrile → HCID 66677560, compound

https://huagongshe.com/reaction/2404353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantPotassium CarbonateHCID 11430—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Methyl-3-(trifluoromethyl)benzonitrileHCID 2775598—
ReactantSarcosine t-butyl ester hydrochlorideHCID 11252350—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 66677560HCID 6667756070%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 4-methyl-3-(trifluoromethyl)benzonitrile (1.85 g, 10 mmol), N-bromosuccinimide (2.14 g, 12.0 mmol) and AIBN (0.033 g, 0.2 mmol) in ACN (40 mL) was heated under reflux for 18 hours. The reaction mixture was diluted with EtOAc and water. The suspension was filtered and the filtrate was separated. The organic phase was washed with brine, dried (MgSO4) and concentrated under vacuum. The residue was purified by flash chromatography (silica, iso-hexane/EtOAc). The material was treated with sarcosine tert-butyl ester hydrochloride (0.516 g, 2.84 mmol) and K2CO3 (0.980 g, 7.1 mmol) in ACN (10 mL). The mixture was heated at 70° C. for 18 hours. The solvent was evaporated under vacuum. The residue was dissolved in a mixture of DCM and water and then poured through a hydrophobic frit. The solvent was evaporated under vacuum. The residue was purified by flash chromatography (silica, iso-hexane/EtOAc) to afford the title compound (0.543 g, 70%). 1H NMR (CDCl3, 400 MHz) δ δ 8.15 (1H, d, J=8.2 Hz), 7.90 (1H, s), 7.83 (1H, d, J=8.2 Hz), 3.90 (2H, s), 3.26 (2H, s), 2.37 (3H, s), 1.48 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802704B2
Source datasetuspto-grants-2014_08
ORD IDord-8ec9e252f7404aa3a03e164fc431f173
Source noteuspto-grants-2014_08