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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50996Generated: October 29, 2026

Benzimidazole → 1-(3-Bromo-1-propyl)benzimidazole

https://huagongshe.com/reaction/50996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzimidazoleHCID 5798—
Reactant1,3-DibromopropaneHCID 8001—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product1-(3-Bromo-1-propyl)benzimidazoleHCID 2225232974%

Reaction Steps

To a solution of benzimidazol (355 mg, 3.00 mmol) in dry DMF (10 mL) was added NaH (83 mg, 3.3 mmol) at 20° C. under N2 atmosphere. The reaction mixture was stirred for 30 min, and then 1,3-dibromopropane (1.82 g, 9.00 mmol) was added and stirres for additional 15 h at 20° C. The reaction was quenched by addition of H2O, and the product was extracted with EtOAc. The organic solution was then washed with H2O and brine, dried over MgSO4, filtered and concentrated in vacuo. 1-(3-Bromo-1-propyl)benzimidazole (530 mg, 74%) was isolated by flash chromatography on a silica gel column by elution with EtOAc/Hexanes a pale yellow oil. 1H NMR (CDCl3, 300 MHz) δ2.40 (qu, 2H, J=6.6 Hz), 3.33 (t, 2H, J=6.2 Hz), 4.42 (t, 2H, J=6.6 Hz), 7.12-7.20 (m, 1H), 7.27-7.48 (m, 2H), 7.43-7.49 (m, 1H), 7.78-7.86 (m, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713471B1
Source datasetuspto-grants-2004_03
ORD IDord-898edd5d828f4588b33757d596d816f7
Source noteuspto-grants-2004_03