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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709518Generated: October 30, 2026

Benzonitrile → HCID 178418369, compound

https://huagongshe.com/reaction/709518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178514644HCID 178514644—
CatalystLithium ChlorideHCID 433294—
SolventDimethylformamideHCID 6228—
ProductHCID 178418369HCID 17841836991.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of benzonitrile (60.0 g, 581.9 mmol, 1.0 equiv) in DMF (anhydrous) (600 mL) was placed in a flask that had been purged and maintained with an inert atmosphere of nitrogen. Ammonium chloride (40.5 g, 757.2 mmol, 1.3 equiv) was added, followed by the addition of lithium chloride (2.0 g, 47.2 mmol, 0.1 equiv). To the mixture was added azidosodium (49.4 g, 756.8 mmol, 1.3 equiv). The resulting solution was stirred overnight, while maintaining the temperature at 100° C. The solids were filtered out and washed with EtOAc. The filtrates were combined and concentrated in vacuo. The residue was dissolved in a 10% NaOH aqueous solution (350 ml). The resulting solution was extracted with EtOAc (100 mL) and the aqueous layers were combined. The pH value of the solution was adjusted to 2 with concentrated HCl. The solids were filtered out and dried over reduced pressure to yield 5-phenyl-1H-tetrazole (78.0 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181206B2
Source datasetuspto-grants-2015_11
ORD IDord-b097904db1b247fb8f991b160eb3c49e
Source noteuspto-grants-2015_11