HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → HCID 10857674, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl alpha-methylbenzeneacetate | HCID 569653 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 10857674 | HCID 10857674 | — |
Reaction Steps
A carbon tetrachloride (150 mL) solution of the intermediate from Step A (10.39 g, 66.6 mmol), N-bromosuccinimide (14.22 g, 80 mmol) and AIBN (0.547 g, 3.33 mmol) was heated to reflux. After 4 hours the reaction solution was cooled to room temperature and the mixture filtered. The filtrate was concentrated and the residue purified by silica gel chromatography using a hexanes/EtOAc gradient to give the indicated product. 1H NMR (500 MHz, CHCl3-d): δ 7.59-7.53 (m, 2H); 7.37-7.30 (m, 3H); 3.80 (s, 3H); 2.31 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365574B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-cbd546dbd502495a83bc811bdc24cd69 |
| Source note | uspto-grants-2016_06 |