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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645212Generated: October 26, 2026

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

https://huagongshe.com/reaction/1645212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-bis(1H-benzimidazol-2-ylmethyl)-N-methylamine chromium (III) chlorideHCID 86638459—
ReactantN,N-bis(1H-benzimidazol-2-ylmethyl)amine chromium (III) chloride hexafluoroantimonate tetrahydrofuranHCID 86638469—
CatalystSilver hexafluoroantimonateHCID 16687962—
SolventTetrahydrofuranHCID 8028—
ProductN,N-bis(1H-benzimidazol-2-ylmethyl)-N-methylamine chromium (III) chloride hexafluoroantimonate tetrahydrofuranHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124698B2
Source datasetuspto-grants-2012_02
ORD IDord-336c3c5f85ed4708815543c78ad05965
Source noteuspto-grants-2012_02