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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362927Generated: October 27, 2026

Sodium Iodide → 1,3-dihydro-1-(3-iodopropyl)-3-methyl-2H-benzimidazol-2-one

https://huagongshe.com/reaction/2362927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-(3-chloropropyl)-3-methyl-1H-benzo[d]imidazol-2(3H)-oneHCID 13360892—
SolventAcetoneHCID 180—
Product1,3-dihydro-1-(3-iodopropyl)-3-methyl-2H-benzimidazol-2-oneHCID 21989977100.1%

Reaction Steps

Sodium iodide (3.43 g, 22.89 mmol, 2 equiv) was added to a solution of 1-(3-chloropropyl)-3-methyl-1H-benzo[d]imidazol-2(3H)-one (2.57 g, 11.44 mmol, 1 equiv) in acetone. The reaction mixture was refluxed for 16 h. After cooling to ambient temperature, it was evaporated under reduced pressure to remove all the acetone. The residue was worked up using ethyl acetate and water, followed by a wash with brine. The organic layer was dried over MgSO4, filtered and concentrated in vacuo to afford the title compound as a red oil (3.62 g, quant); 1H NMR (400 MHz, DMSO-d6): δ 2.12-2.19 (m, 2H); 3.24 (t, 2H, J=7.2 and 6.8 Hz); 3.28 (s, 3H); 3.89 (t, 2H, J=6.8 Hz); 7.04-7.09 (m, 2H); 7.13-7.16 (m, 1H); 7.18-7.22 (m, 1H); MS for C11H13IN2O m/z 316.89 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691836B2
Source datasetuspto-grants-2014_04
ORD IDord-87b906942fb94154a7560228bbe15f7b
Source noteuspto-grants-2014_04