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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 2-Bromobenzonitrile | HCID 16272 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(2-Bromophenyl)-1H-tetrazole | HCID 178419373 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05164403 |
|---|
| Source dataset | uspto-grants-1992_11 |
|---|
| ORD ID | ord-17fc21c95b2244369c743ae3ea210cd4 |
|---|
| Source note | uspto-grants-1992_11 |
|---|