HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 5-(4-bromophenyl)-2-(1,1-dimethylethyl)-2H-tetrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 5-(4-Bromophenyl)-1H-tetrazole | HCID 766141 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5-(4-bromophenyl)-2-(1,1-dimethylethyl)-2H-tetrazole | HCID 14888728 | 71% |
Reaction Steps
5-(4-Bromophenyl)-2H-tetrazole (19.0 g, 81.9 mmol), t-butanol (12.1 g, 164 mmol), trifluoroacetic acid (80 mL) and concentrated sulfuric acid (4.6 g, 41 mmol) were stirred at ambient temperature for 24 hours. The mixture was concentrated and dissolved in ethyl acetate (200 mL). After washing with water (3×25 mL), 1M NaOH (3×25 mL) and brine (25 mL) the organic layer was dried (Na2SO4), filtered and concentrated. The oil was purified by chromatography on a Waters Prep 500 liquid chromatograph fitted with two silica gel cartridges eluting with a mixture of hexanes and ethyl acetate (9:1) to provide 5-(4-bromophenyl)-2-(1,1-dimethylethyl)-2H-tetrazole (17.1 g, 58.1 mmol) as a yellow oil in 71% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05508437 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-077b45e8dbef4b10a33a72cd8661f864 |
| Source note | uspto-grants-1996_04 |