HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → N'-hydroxy-3H-benzimidazole-5-carboximidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | HCID 178509527 | HCID 178509527 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N'-hydroxy-3H-benzimidazole-5-carboximidamide | HCID 178513241 | 93.4% |
Reaction Steps
To a suspension of 1H-benzimidazole-5-carbonitrile obtained in step 1 (1 g; 6.99 mmol) in EtOH (20 mL) was added hydroxylamine (50% in water, 2.10 mL; 34.93 mmol) and the mixture was stirred at RT for 36 hours. The solution was concentrated under vacuum to give the title compound as a light pink solid (1.15 g, 93%). 1H NMR (DMSO-d6): δ 12.52 (br s, 1H), 9.51 (s, 1H), 8.23 (s, 1H), 7.89 (br s, 1H), 7.56 (s, 2H), 5.80 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08741923B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-45500b74b35c4087b882fdac84bc987e |
| Source note | uspto-grants-2014_06 |