Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Triethylamine hydrochloride | HCID 11130 | — |
| Edukt | 3-Nitrobenzonitrile | HCID 12079 | — |
| Edukt | Sodium Azide | HCID 33557 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | 5-(3-nitrophenyl)tetrazole | HCID 285129 | 88,9% |
Reaktionsschritte
To a solution of 3-cyanonitrobenzene-(20 g, 0.13 mol) in 1-methyl-2-pyrrolidinone (200 ml) was added triethylamine hydrochloride (27.9 g, 0.20 mol) followed by sodium azide (26.4 g, 0.40 mol). The mixture was heated at 160° C. for 1.5 h, then cooled to ambient temperature, poured into ice water (1000 ml) and acidified using 5M HCl. The solid which precipitated from the mixture was filtered, washed with water and dried under vacuum at 50° C. to afford the title tetrazole (22.1 g, 86%) as a beige powder; mp 154°-156° C; δH (360 MHz, CDCl3), 7.59 (1H, t, J=9 Hz), 8.19 (1H, d, J=8 Hz), 8.36 (1H, d, J=8 Hz), 8.86 (1H, s).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05521175 |
|---|
| Quelldatensatz | uspto-grants-1996_05 |
|---|
| ORD ID | ord-3d319f418d134ab0a512648139f0bdff |
|---|
| Quellennotiz | uspto-grants-1996_05 |
|---|