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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 3-Tetradecylthioacetylamino-1-triphenylmethyloxypropan-2-ol | HCID 86603210 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Iodo-3-tetradecylthioacetylamino-1-triphenylmethyloxypropane | HCID 87831810 | 21% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253296B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-e9cd72ba806f4867b91d5d9fb0a48916 |
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| Source note | uspto-grants-2007_08 |
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