HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → HCID 22256031, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22256033 | HCID 22256033 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 22256031 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06989462B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-a4133ec2e945442d94b3b24fe5aea726 |
| Source note | uspto-grants-2006_01 |