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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373619Generated: October 30, 2026

Hydrochloric Acid → 5-(2-Bromophenyl)-1H-tetrazole

https://huagongshe.com/reaction/373619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTributyltin ChlorideHCID 15096—
Reactant2-BromobenzonitrileHCID 16272—
ReactantSodium AzideHCID 33557—
SolventO-XyleneHCID 7237—
SolventTetrahydrofuranHCID 8028—
Product5-(2-Bromophenyl)-1H-tetrazoleHCID 17841937376%

Reaction Steps

A 64 g (350 mmol) sample of 2-bromobenzonitrile (Aldrich) was dissolved in 650 mL of xylene and treated with 22.75 g (350 mmol) of sodium azide and 95 mL (350 mmol) of tributyltin chloride at reflux for 48 h. The reaction was filtered; the filtrate was treated with 50 mL of anhydrous tetrahydrofuran (THF) and 20 g (550 mmol) of hydrogen chloride. The reaction was stirred for 2 h; filtration gave 59.6 g (76%) of 5-(2-bromophenyl)-1H-tetrazole: mp 178-180° C.; NMR (DMSO-d6) δ 7.50-7.64 (m, 2H), 7.67-7.74 (m, 1H), 7.83-7.91 (m, 1H). A 41.8 g (187 mmol) sample of this material was dissolved in 650 mL of methylene chloride and treated with 55.5 g (193 mmol) of triphenylmethyl chloride and 30 mL (220 mmol) of anhydrous triethylamine. The reaction was stirred overnight at reflux, cooled to ambient temperature, washed with water,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05164403
Source datasetuspto-grants-1992_11
ORD IDord-17fc21c95b2244369c743ae3ea210cd4
Source noteuspto-grants-1992_11