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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645203Generated: October 31, 2026

N,N-bis(1H-benzimidazol-2-ylmethyl)-N-methylamine → N,N-bis(1H-benzimidazol-2-ylmethyl)-N-methylamine chromium (III) chloride

https://huagongshe.com/reaction/1645203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-bis(1H-benzimidazol-2-ylmethyl)-N-methylamineHCID 59460—
ReactantPotassium BromideHCID 253877—
ReactantN,N-bis(1H-benzimidazol-2-ylmethyl)amine chromium (III) chlorideHCID 86638460—
SolventDimethylformamideHCID 6228—
ProductN,N-bis(1H-benzimidazol-2-ylmethyl)-N-methylamine chromium (III) chlorideHCID 86638459—

Reaction Steps

3b was synthesised by an analogous procedure to that described for 3a using 2b (2 g, 6.87 mmol) and CrCl3(THF)3 (2.57 g, 6.87 mmol). Yield 2.87 g (93%). Anal. Calc. for C17H17Cl3CrN5 (in %): C, 45.40; H, 3.81; N, 15.57. Found C, 45.35; H, 3.76; N, 15.66. IR (KBr, cm−1), υ 3221 (NH, s), υ 1622-1544 (ArC═C, C═N, m), δ 1455, 1477, 1497 (N—H, s), υ 1274 (CN, s), δ 753 (CH, s). UV-VIS (DMF, 298 K): λmax/nm (εmax/dm3 mol−1 cm−1)=464 (156), 659 (75), 723 (shoulder). +FAB-MS: (m/z): 413 ([M-Cl]+), 291 ([M-CrCl3]). μeff·=3.60 MB.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124698B2
Source datasetuspto-grants-2012_02
ORD IDord-37c3fcfdf1534acb9c836cb377039033
Source noteuspto-grants-2012_02