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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751003Generated: October 27, 2026

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

https://huagongshe.com/reaction/1751003

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 u 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 numberUS09156840B2
Source datasetuspto-grants-2015_10
ORD IDord-43788f393a8d49709fe3309f4384f0b8
Source noteuspto-grants-2015_10