HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → HCID 131718089, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 131718090 | HCID 131718090 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 131718089 | HCID 131718089 | — |
Reaction Steps
To a solution of N-Triphenylmethyl-5-(4-fluoro-4'-methyl-biphen-2-yl)tetrazole (454.4 mg; 0.9161 mmol) in dry CCl4 (8 mL) was added N-bromosuccinimide (179.2 mg; 1.1 eq) and a catalytic amount of AIBN. The reaction was heated to reflux (105°-115°) under N2. After 3 hrs. the reaction was cooled and filtered through a cotton plugged pipet to remove the succinimide formed. The solvent was removed and replaced by EtOAc/Et2O. The reaction was washed with 1N NaOH and brine. The organic solution was dried over anhydrous MgSO4, filtered, and concentrated in vacuo to afford the product. The crude product was used in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05240928 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-4138e63ce9414e8cb4788aea39893571 |
| Source note | uspto-grants-1993_08 |