HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651502Generated: October 27, 2026
Imidazole → 1,1,1,2,2-Pentafluoro-5-iodopentane
https://huagongshe.com/reaction/651502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4,4,5,5,5-Pentafluoropent-2-en-l-ol | HCID 54452699 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1,1,2,2-Pentafluoro-5-iodopentane | HCID 12017057 | — |
Reaction Steps
446 mg of triphenylphosphine is dissolved in 2 cm3 of methylene chloride, cooled down to 10° C., 116 mg of imidazole is added, agitation is carried out for 15 minutes, 431 mg of iodine is added, agitation is carried out for 30 minutes, 0.21 cm3 of 4,4,5,5,5-pentafluoro 2-penten 1-ol is added, agitation is carried out for 4 hours at ambient temperature, the organic phase is washed with a saturated aqueous solution of sodium thiosulphate and a chloromethylenic solution of 4,4,5,5,5-pentafluoro iodopentane is obtained which is used as it is in the continuation of the synthesis. The operation is carried out as indicated in Example 8 Stage F, starting with 618 mg of the thioacetate prepared below in 7 cm3 of methanol and the chloromethylenic solution of the iodated derivative prepared above. 1.2 g of expected product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06281204B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-27cc0f16930b48fc9666833cc792af8f |
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| Source note | uspto-grants-2001_08 |
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