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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416653Generated: October 30, 2026

2-(1H-benzimidazol-2-yl)aniline → HCID 12668461, compound

https://huagongshe.com/reaction/416653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(1H-benzimidazol-2-yl)anilineHCID 79869—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12668461HCID 12668461—

Reaction Steps

2-(1H-benzo[d]imidazol-2-yl)benzenamine (525 mg, 2.5 mmol) in 5 mL dry THF was cooled to −78 degrees before 1 mL n-Bu—Li (2.5 mmol, 2.5 N in hexanes) was added via a syringe. The reaction was stirred at −78 degrees for 20 min and Mel (360 mg, 2.6 mmol) was added. The reaction was warmed to r.t. gradually and kept at room temperature for another hour. The reaction crude was diluted with 25 mL ether and the resulted suspension was filtered off the solid. The crude product was isolated after the solvent was removed from the collected filtrate to product 510 mg of 2-(1-methyl-1H-benzo[d]imidazol-2-yl)benzenamine in greater than 95% purity (MS, M++H=224.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088928B2
Source datasetuspto-grants-2012_01
ORD IDord-cf5d1fa3010a4760a8a186b7175951a7
Source noteuspto-grants-2012_01