HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384413Generated: October 26, 2026
Iodine chloride → 2,2,2-trichloro-1-(4-iodo-1H-pyrrol-2-yl)ethan-1-one
https://huagongshe.com/reaction/384413
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | 2-(Trichloroacetyl)pyrrole | HCID 321487 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2,2-trichloro-1-(4-iodo-1H-pyrrol-2-yl)ethan-1-one | HCID 11681602 | 92% |
Reaction Steps
2,2,2-Trichloro-1-(1H-pyrrol-2-yl)-ethanone 57b (32 g, 151.8 mmol) was dissolved in 250 mL of dichloromethane followed by dropwise addition of a solution of iodine monochloride (25 g, 153 mmol) in 125 mL of dichloromethane. Upon completion of the addition, the reaction mixture was stirred at room temperature for 2 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was washed with saturated aqueous sodium carbonate, aqueous sodium thiosulfate (2 M) and saturated brine successively, dried over anhydrous magnesium sulfate, filtered to remove the drying agent and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound 2,2,2-trichloro-1-(4-iodo-1H-pyrrol-2-yl)-ethanone 57c (47 g, yield 92%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367710B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-4294c4f831524387a01874cba807fb65 |
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| Source note | uspto-grants-2013_02 |
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