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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481759Generated: October 30, 2026

Benzonitrile → HCID 178418369, compound

https://huagongshe.com/reaction/481759

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 numberUS05789587
Source datasetuspto-grants-1998_08
ORD IDord-8eca110288f744d997266c172ef3d46e
Source noteuspto-grants-1998_08