Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452027Generated: October 30, 2026

Benzonitrile → HCID 178418369, compound

https://huagongshe.com/reaction/1452027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
ReactantSodium AzideHCID 33557—
CatalystZincchlorideHCID 3007855—
ProductHCID 178418369HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05606054
Source datasetuspto-grants-1997_02
ORD IDord-e7262c0c14be4395913fed1a7d13e760
Source noteuspto-grants-1997_02