Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853204Generated: October 31, 2026

Imidazole → 2-Iodo-3-tetradecylthioacetylamino-1-triphenylmethyloxypropane

https://huagongshe.com/reaction/853204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BisulfiteHCID 23665763—
Reactant3-Tetradecylthioacetylamino-1-triphenylmethyloxypropan-2-olHCID 86603210—
SolventTolueneHCID 1140—
Product2-Iodo-3-tetradecylthioacetylamino-1-triphenylmethyloxypropaneHCID 8783181021%

Reaction Steps

3-tetradecylthioacetylamino-1-triphenylmethyloxypropan-2-ol (example 20a) (2 g, 3.31 mmol) was dissolved in toluene (100 ml). Imidazole (0.564 g, 8.28 mmol), triphenylphosphine (2.171 g, 8.28 mmol) and iodine (1.681 g, 6.62 mmol) were then added in that order. The reaction medium was stirred at room temperature for 20 hours. A saturated sodium bisulfite solution was added until complete blanching of the reaction medium. The phases were separated and the aqueous phase was extracted with toluene. The organic phases were combined, washed with saturated sodium chloride solution, dried on magnesium sulfate and filtered. The residue obtained after evaporation of the solvent (4.65 g) was purified by chromatography on silica gel (eluent: dichiromethane) to give the desired compound in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253296B2
Source datasetuspto-grants-2007_08
ORD IDord-e9cd72ba806f4867b91d5d9fb0a48916
Source noteuspto-grants-2007_08