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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538842Generated: October 27, 2026

Benzonitrile → HCID 178418369, compound

https://huagongshe.com/reaction/538842

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, 1.00 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, 1.30 equiv) was added, followed by the addition of lithium chloride (2.0 g, 47.2 mmol, 0.08 equiv). To the mixture was added azidosodium (49.4 g, 756.8 mmol, 1.30 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 under vacuum. The residue was dissolved in 350 ml of 10% NaOH aqueous solution. The resulting solution was extracted with 100 mL of EtOAc 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 78.0 g (91%) of 5-phenyl-1H-tetrazole as a white solid. ES m/z: [M+H]+ calcd for C7H6N4, 147.1. found 147.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865755B2
Source datasetuspto-grants-2014_10
ORD IDord-d2cd549f172042bab716119e3fc854f6
Source noteuspto-grants-2014_10