HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539619Generated: October 25, 2026
Imidazole → [1-(4-Fluoro-phenyl)-2-iodo-ethyl]-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/539619
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphane dichloride | HCID 13797396 | — |
| Reactant | Tert-butyl [1-(4-fluorophenyl)-2-hydroxyethyl]carbamate | HCID 58200246 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [1-(4-Fluoro-phenyl)-2-iodo-ethyl]-carbamic acid tert-butyl ester | HCID 58200314 | 58% |
Reaction Steps
To a room temperature solution of triphenylphosphine dichloride (1.53 g (5.85 mmol) in methylene chloride was added iodine (1.481 g, 5.85 mmol). The mixture was stirred for fifteen minutes, then imidazole (663 mg, 9.74 mmol) was added. The mixture was stirred another 15 minutes, then [1-(4-fluoro-phenyl)-2-hydroxy-ethyl]carbamic acid tert-butyl ester (1.0 g, 3.9 mmol) was added. The mixture was heated to reflux for two hours, then stirred at room temperature overnight. Solvent was removed under reduced pressure, and the residue was partitioned between ethyl acetate and saturated aqueous sodium thiosulfate. The organic layer was separated, washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was chromatographed through silica (5-10% ethyl acetate/hexanes) to give 820 mg (58%) of [1-(4-fluoro-phenyl)-2-iodo-ethyl]-carbamic acid tert-butyl ester, MP=138-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871760B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-4d1d6fe8d4b04a86b69a86abb67c3011 |
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| Source note | uspto-grants-2014_10 |
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