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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693042Generated: November 4, 2026

Sodium Iodide → (5-Iodo-pentyl)-cyclohexane

https://huagongshe.com/reaction/1693042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant(5-Bromopentyl)cyclohexaneHCID 14952366—
SolventAcetoneHCID 180—
Product(5-Iodo-pentyl)-cyclohexaneHCID 5898581356.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of (5-bromo-pentyl)-cyclohexane (2 gm, 8.58 mmol) in acetone (20 ml), and sodium iodide (2.57 g, 17.15 mmol) was heated at 60° C. for 12 hrs and then cooled to room temperature. The solvent was evaporated, the residue was taken up in EtOAc (30 ml), washed with water (20 ml) and then brine (30 ml). The organic layer was separated, dried over anhydrous sodium sulfate and solvent was removed under reduced pressure. The crude product was purified by column chromatography using hexane as an eluent to yield an oily liquid (1.36 gm). 1H NMR (CDCl3): δ 0.8 (t, 2H, J=10.2 Hz), 1.00-1.38 (m, 9H), 1.52-168 (m, 6H), 1.70-1.80 (m, 2H), 3.10 (t, 2H, J=6.9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158646B2
Source datasetuspto-grants-2012_04
ORD IDord-e4449c8d7f934536906728219e3fe949
Source noteuspto-grants-2012_04