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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721231Generated: November 3, 2026

Ammonium Chloride → 5-((4-bromophenyl)methyl)-1H-1,2,3,4-tetrazole

https://huagongshe.com/reaction/1721231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzeneacetonitrile, 4-bromo-HCID 27914—
ReactantSodium AzideHCID 33557—
SolventDimethylformamideHCID 6228—
Product5-((4-bromophenyl)methyl)-1H-1,2,3,4-tetrazoleHCID 1488870046.7%

Reaction Steps

4-Bromophenylacetonitrile (30.0 g, 0.15 mol), sodium azide (10.9 g, 0.17 mol) and ammonium chloride (8.9 g, 0.17 mol) were heated in DMF (300 mL) at 90° C. for 2 days. After concentration, water (200 mL) was added to the residue, the mixture was basified with 1M NaOH (170 mL) and washed with ether (2×100 mL). Acidification of the aqueous layer with 1N HCl and collection of the precipitate by suction filtration produced the crude product. This was purified by recrystallization from ethanol to provide 5-[(4-bromophenyl)methyl]-2H-tetrazole (17.2 g, 0.07 mol) in 44% yield, mp. 173°-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508437
Source datasetuspto-grants-1996_04
ORD IDord-4502ab9a12494cd69c7a8e3b66cc24bc
Source noteuspto-grants-1996_04