HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Chloro-2-(1H-tetrazol-1-YL)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 5-Chloro-2-(1H-tetrazol-1-YL)benzamide | HCID 21866169 | — |
| Reactant | (Methoxycarbonylsulfamoyl)ammonium hydroxide | HCID 21866229 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-2-(1H-tetrazol-1-YL)benzonitrile | HCID 21866280 | 90% |
Reaction Steps
To a solution of 5-chloro-2-(1H-tetrazol-1-yl)benzamide (1.0 g, 4.5 mmol) in THF (29 mL) was added (methoxycarbonylsulfamoyl)ammonium hydroxide, inner salt (2.1 g, 8.8 mmol) in five portions over 5 h. Water was added and the reaction mixture was extracted with ethyl acetate. The combined organic layers were washed with brine. Drying and solvent evaporation gave 5-chloro-2-tetrazol-1-yl-benzonitrile (0.83 g, 90%); 1H NMR (400 MHz, CDCl3): δ 9.26 (s, 1H), 7.90 (d, J=1.0 Hz, 1H,), 7.85 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07144899B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-123854651c78421f8042803bb89f28d7 |
| Source note | uspto-grants-2006_12 |