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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645209Generated: October 30, 2026

Potassium Bromide → N,N-bis(1H-benzimidazol-2-ylmethyl)-N-phenylamine chromium (III) chloride

https://huagongshe.com/reaction/1645209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantN,N-bis(1H-benzimidazol-2-ylmethyl)-N-phenylamineHCID 66775276—
ReactantN,N-bis(1H-benzimidazol-2-ylmethyl)amine chromium (III) chlorideHCID 86638460—
SolventDimethylformamideHCID 6228—
ProductN,N-bis(1H-benzimidazol-2-ylmethyl)-N-phenylamine chromium (III) chlorideHCID 86638465—

Reaction Steps

3h was synthesised by an analogous procedure to that described for 3a using N,N-bis(1H-benzimidazol-2-ylmethyl)-N-phenylamine (0.20 g, 0.56 mmol) and CrCl3(THF)3 (0.21 g, 0.56 mmol). Yield 0.23 g (87%). Anal. Calc. for C22H19Cl3CrN5 (in %): C, 51.63; H, 3.74; N, 13.68. Found C, 51.49; H, 4.95; N, 13.58. IR (KBr, cm−1), υ 3224 (NH, s), υ 1637-1540 (ArC═C, C═N, m), δ 1454, 1477, 1498 (N—H, s, m), υ 1275 (CN, s), δ 748 (CH, s). UV-VIS (DMF, 298 K): λmax/nm=484, 678, 707 (shoulder). +FAB-MS: (m/z): 475 ([M-Cl]+), δ 440 ([M-2Cl]), 354 ([M-CrCl3]+). μeff·=3.95 MB.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124698B2
Source datasetuspto-grants-2012_02
ORD IDord-af434b7ae4064b88ab9fb6e122afbb9b
Source noteuspto-grants-2012_02