HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220177Generated: October 29, 2026
Dimethylformamide → 4-Iodo-1-tritylimidazole
https://huagongshe.com/reaction/2220177
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-iodo-1H-imidazole | HCID 2773468 | — |
| Product | 4-Iodo-1-tritylimidazole | HCID 618252 | — |
Reaction Steps
DMF, 100 mL, was stirred, and 13.2 grams (0.068 mole) of 5-iodoimidazole (vi) was added, followed by 18.9 grams (0.068 mole) of triphenylmethyl chloride, and 3.3 grams (0.033 mole) of triethylamine. Upon completion of addition, the reaction mixture was stirred at ambient temperature for 18 hours. After this time, the reaction mixture was poured into crushed ice where it stirred until the ice melted. The resultant solid was then collected by filtration and triturated with diethyl ether. A solid was collected by filtration and washed with diethyl ether, yielding the subject compound. The diethyl ether filtrate was concentrated under reduced pressure to a residue, and re-triturated with diethyl ether, yielding additional subject compound. The total yield of subject compound was about 5.0 grams. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07417057B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-6890e701de3048d6b53ff75e56a0df8d |
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| Source note | uspto-grants-2008_08 |
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