HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213330Generated: October 30, 2026
Azidotrimethylsilane → HCID 178509700, compound
https://huagongshe.com/reaction/2213330
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azidotrimethylsilane | HCID 78378 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 14929112 | HCID 14929112 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178509700 | HCID 178509700 | — |
Reaction Steps
3-[(E)-2-Nitroethenyl]benzonitrile (2.79 g, 16.0 mmol) and azidotrimethylsilane (2.76 g, 24.0 mmol) was stirred in anhydrous DMF (100 mL) at 50° C. To this was added tetrabutylammonium fluoride (17.6 mL of a 1.0M solution in THF, 17.6 mmol) via syringe pump over 20 min. The resulting reaction was quenched with MeOH (25 mL) and concentrated in vacuo to a volume of ca. 30 mL. The resulting crude mixture was dissolved in EtOAc (300 mL) and washed with H2O (2×100 mL). The product was then extracted from the EtOAc layer with 1M aqueous NaOH (4×75 mL). The combined basic aqueous portions were treated with 4M HCl to obtain an endpoint of pH=4, and the product was extracted into EtOAc (4×100 mL). The combined EtOAc extracts were dried (MgSO4), filtered and concentrated in vacuo to obtain 3-(1H-1,2,3-triazol-4-yl)benzonitrile as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07105548B2 |
|---|
| Source dataset | uspto-grants-2006_09 |
|---|
| ORD ID | ord-885792a93bfa466e84b5687b9e54e493 |
|---|
| Source note | uspto-grants-2006_09 |
|---|