HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → N,N-bis(1H-benzimidazol-2-ylmethyl)-N-cyclohexylamine chromium (III) chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | N,N-bis(1H-benzimidazol-2-ylmethyl)amine chromium (III) chloride | HCID 86638460 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,N-bis(1H-benzimidazol-2-ylmethyl)-N-cyclohexylamine chromium (III) chloride | HCID 86638464 | — |
Reaction Steps
3g was synthesised by an analogous procedure to that described for 3a using 2g (1 g, 2.79 mmol) and CrCl3(THF)3 (1.04 g, 2.79 mmol). Yield 1.07 g (74%). Anal. Calc. for C22H25Cl3CrN5 (in %): C, 51.03; H, 4.87; N, 13.52. Found C, 50.93; H, 4.71; N, 13.64. IR (KBr, cm−1), υ 3225 (NH, s), υ 1623-1540 (ArC═C, C═N, m), δ 1455, 1478, 1496 (N—H, s, m), υ 1276 (CN, m), δ 750 (CH, s). UV-VIS (DMF, 298 K): λmax/nm (εmax/dm3 mol−1 cm−1)=459 (160), 704 (65), 733 (shoulder). +FAB-MS: (m/z): 481 ([M-Cl]+), 446 ([M-2Cl]), 360 ([M-CrCl3]). μeff·=3.88 MB.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124698B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-272190a801054bfeb8910d0dbd7ccb07 |
| Source note | uspto-grants-2012_02 |