HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzonitrile → HCID 178418369, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | HCID 178418369 | HCID 178418369 | — |
Reaction Steps
As outlined in Scheme 8, benzonitrile is treated with sodium azide and zinc chloride to give 5-phenyltetrazole 14 which is converted to the N-trityl derivative 15 by treatment with triphenylmethyl chloride and triethylamine. The zinc reagent 16 was prepared by treatment with n-butyllithium followed by zinc chloride. Coupling with 4-iodotoluene using the catalyst bis(triphenylphosphine)nickel(II) dichloride gives the biphenyl product 17 in high yield. Treatment with N-bromosuccinimide in refluxing carbon tetrachloride, in the presence of a radical initiator such as benzoyl peroxide or 2,2'-azobisisobutyronitrile (AIBN), gives bromide 18.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05789587 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-8eca110288f744d997266c172ef3d46e |
| Source note | uspto-grants-1998_08 |