HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539436Generated: October 31, 2026
Nitrogen → 2-Iodo-1h,1h,2h,3h,3h-perfluoroalkan-1-ol (linear)
https://huagongshe.com/reaction/539436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Trifluoroiodomethane | HCID 16843 | — |
| Reactant | Fluorine | HCID 24524 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Iodo-1h,1h,2h,3h,3h-perfluoroalkan-1-ol (linear) | HCID 119095585 | — |
Reaction Steps
Into a 3-liter autoclave were poured 174 g (3.0 mol) of allyl alcohol, 49.2 g (0.3 mol) of α,α′-azobis isobutyronitrile (AIBN) and 300 ml of ethyl acetate. After decreasing the inside pressure (100 mmHg) on ice bath, N2 was introduced, and the inside pressure was decreased again. Thereafter, 588 g (3.0 mol) of CF3I was introduced and the mixture was slowly heated up to 60° C. After completion of the reaction, the reaction solution was cooled and washed with 1 mol/liter of an aqueous solution of HCl for separation of the solution. After that, refining by distillation was carried out, and 533 g (2.1 mol) of a fluorine-containing iodide (a): CF3CH2CHICH2OH was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08871384B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-7c7099b134c74f8f8dec90527b2bbf6a |
|---|
| Source note | uspto-grants-2014_10 |
|---|