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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628220Generated: October 25, 2026

Imidazole → 9-(Iodomethyl)nonadecane

https://huagongshe.com/reaction/628220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant2-OctyldodecanolHCID 21414—
ReactantSodium SulfiteHCID 24437—
SolventDichloromethaneHCID 6344—
Product9-(Iodomethyl)nonadecaneHCID 8669145092.9%

Reaction Steps

Iodine (12.25 g, 48.3 mmol) was added to a solution of 2-octyl-1-dodecanol (12.42 g, 41.6 mmol), triphenylphosphine (13.17 g, 50.2 mmol), and imidazole (3.42 g, 50.2 mmol) in 80 mL dichloromethane at 0° C. After stirring for 30 minutes, the reaction mixture was allowed to warm to room temperature over 4 hours before 12 mL of saturated Na2SO3 (aq) was added. The organics were concentrated by evaporation and the mixture taken up in 500 mL pentane, washed three times with 200 mL water, and once with 150 mL brine. The mixture was then passed through a 3 cm silica gel plug, and dried over Na2SO4. The organics were concentrated by evaporation to give a colorless oil (15.78 g, yield 92.9%). 1H NMR (CDCl3 500 MHz): δ: 2.60 (d, J=5.0 Hz, 2H), 2.00 (t, J=5.0 Hz, 1H), 1.30-1.20 (b, 32H), 0.89 (t, J=7.5 Hz, 6H); MS (EI): m/z (%) 408.23 (100) [M+]. Elemental Analysis (calc. C, 58.81; H, 10.12): found C, 58.70; H, 9.97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09312492B2
Source datasetuspto-grants-2016_04
ORD IDord-3824af1174994d87889bc1a111ee3b6b
Source noteuspto-grants-2016_04