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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645205Generated: October 30, 2026

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

https://huagongshe.com/reaction/1645205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantN,N-bis(1H-benzimidazol-2-ylmethyl)-N-benzylamineHCID 21107922—
ReactantN,N-bis(1H-benzimidazol-2-ylmethyl)amine chromium (III) chlorideHCID 86638460—
SolventDimethylformamideHCID 6228—
ProductN,N-bis(1H-benzimidazol-2-ylmethyl)-N-benzylamine chromium (III) chlorideHCID 86638462—

Reaction Steps

3d was synthesised by an analogous procedure to that described for 3a using 2d (0.63 g, 1.73 mmol) and CrCl3(THF)3 (0.65 g, 1.73 mmol). Yield 0.79 g (88%). Anal. Calc. for C23H21Cl3CrN5 (in %): C, 52.54; H, 4.03; N, 13.32. Found C, 52.43; H, 4.03; N, 13.23. IR (KBr, cm−1), υ 3255 (NH, s), υ 1617-1550 (ArC═C, C═N, m), δ 1454, 1477, 1496 (N—H, s, m), υ 1276 (CN, s), δ 749 (CH, s). UV-VIS (DMF, 298 K): λmax/nm (εmax/dm3 mol−1 cm−1)=462 (162), 665 (75), 726 (shoulder). +FAB-MS: (m/z): 489 ([M-Cl]+), 454 ([M-2Cl]), μμeff·=4.00 MB.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124698B2
Source datasetuspto-grants-2012_02
ORD IDord-942cebd2d0b14c5e8a26c6d091ab42f4
Source noteuspto-grants-2012_02