HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-bis(1H-benzimidazol-2-ylmethyl)-N-methylamine chromium (III) chloride → N,N-bis(1H-benzimidazol-2-ylmethyl)-N-methylamine chromium (III) chloride hexafluoroantimonate tetrahydrofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-bis(1H-benzimidazol-2-ylmethyl)-N-methylamine chromium (III) chloride | HCID 86638459 | — |
| Reactant | N,N-bis(1H-benzimidazol-2-ylmethyl)amine chromium (III) chloride hexafluoroantimonate tetrahydrofuran | HCID 86638469 | — |
| Catalyst | Silver hexafluoroantimonate | HCID 16687962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N-bis(1H-benzimidazol-2-ylmethyl)-N-methylamine chromium (III) chloride hexafluoroantimonate tetrahydrofuran | HCID 86638468 | — |
Reaction Steps
4b was synthesised by an analogous procedure to that described for 4a using silver hexafluoroantimonate (0.762 g, 2.22 mmol) and complex 3b (1 g, 2.22 mmol). Yield 1.09 g, 72%. Anal. Calc. for C21H25Cl2CrF6N5OSb: C, 34.93; H, 3.49; N, 9.70. Found C, 34.89; H, 3.58; N, 9.58. IR (cm−1), υ 3220 (NH, s), υ 3050 (Ar—H, s), υ 1597 (ArC═C, m), δ 1480, 1457 (N—H, m), υ 1277 (CN, m), δ 753 (CH, s), υ 664 (Sb—F, s). FAB(+) mass spectrum, m/z 413 [M+-THF], 378 ([M+-Cl, THF], 288 [M+-Cr(THF)C2]. FAB(−) mass spectrum, m/z 235 [M−]. μeff·=3.77 MB.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124698B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-336c3c5f85ed4708815543c78ad05965 |
| Source note | uspto-grants-2012_02 |