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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantAllyl AlcoholHCID 7858—
ReactantTrifluoroiodomethaneHCID 16843—
ReactantFluorineHCID 24524—
ReactantIodide IonHCID 30165—
SolventEthyl AcetateHCID 8857—
Product2-Iodo-1h,1h,2h,3h,3h-perfluoroalkan-1-ol (linear)HCID 119095585—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871384B2
Source datasetuspto-grants-2014_10
ORD IDord-7c7099b134c74f8f8dec90527b2bbf6a
Source noteuspto-grants-2014_10