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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353023Generated: October 30, 2026

Acetonitrile → HCID 131726456, compound

https://huagongshe.com/reaction/1353023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantAzobisisobutyronitrileHCID 6547—
Reactant1,1,2,2,3,3,4,4-Octafluoro-1,4-diiodobutaneHCID 78993—
SolventDichloromethaneHCID 6344—
ProductHCID 131726456HCID 131726456—

Reaction Steps

The procedure of Example 17 was followed, except solvent and initiator were varied. Due to the well-known unsuitability of CH2Cl2 as a solvent in regular free radical polymerization systems, including AIBN case, the solvent was changed to acetonitrile. After adding 0.3 g of AIBN, 0.8 g of I(CF2)4I, 3.0 g of CF2═CFCH2CH2OSi(CH3)3, and 30 ml of acetonitrile in a 70 ml stainless autoclave equipped with a magnetic stirrer, 20 ml of VDF and 5 ml of HFP were introduced into the reactor under vacuum by condensing the monomers at liquid nitrogen temperatures. The autoclave was warmed to room temperature gradually and then immersed in an oil bath at 70° C. for 20 hours. After recovering the unreacted monomers, clear solution was observed, and only trace amount (<0.1 g) of white powder was obtained after removing the volatiles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220807B2
Source datasetuspto-grants-2007_05
ORD IDord-a8767bf856734c27b95f0f8786728a2e
Source noteuspto-grants-2007_05