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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611747Generated: November 1, 2026

Azobisisobutyronitrile → HCID 22256031, compound

https://huagongshe.com/reaction/1611747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantSulfuryl chlorideHCID 24648—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22256033HCID 22256033—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 22256031HCID 22256031—

Reaction Steps

12.0 g of benzyl 2,6-dimethylbenzoate are initially charged into 50 ml of carbon tetrachloride admixed at room temperature with 5.4 g of sulfuryl chloride and 40 mg of AIBN. The mixture is stirred at reflux for 4–5 h. Afterwards, it is admixed with 40 ml of saturated NaHCO3 solution. After the phase separation, the organic phase is washed with 50 ml of 10% sodium sulfite solution, and the organic phase is then dried over magnesium sulfate. The product-containing solution is filtered trough silica gel and washed again with 20 ml of carbon tetrachloride. After distilling off the solvent in vacuo, the product obtained is a bright yellow oil. Yield: 8.0 g (73% of theory; 88.4 area %).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06989462B2
Source datasetuspto-grants-2006_01
ORD IDord-a4133ec2e945442d94b3b24fe5aea726
Source noteuspto-grants-2006_01