HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 6,6,7,7,8,8,9,9,9-Nonafluorononan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorous acid | HCID 107909 | — |
| Reactant | HCID 85830369 | HCID 85830369 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6,6,7,7,8,8,9,9,9-Nonafluorononan-1-ol | HCID 15415175 | — |
Reaction Steps
A solution of AIBN (4.9 g, 30 mmol) in dioxane (150 cm3) was added dropwise into a solution of 4iodo-6,6,7,7,8,8,9,9,9-nonafluorononan-1-ol (Preparation 1B, 25 g, 58 mmol), phosphorous acid (19.1 g, 0.29 mol) and triethylamine (32.3 g, 0.32 mol) in dioxane (150 cm3) under an atmosphere of nitrogen during reflux. After addition, the reaction mixture was refluxed for a period of time until the GLC analysis revealed a complete reaction (usually an hour). The crude product was extracted into diethyl ether (3×50 cm3) and dried (MgSO4). The solvent was removed in vacuo and the pure product was obtained by reduced pressure distillation as a colourless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351452B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-20f6b7d6954c4d52918c4cde540dc912 |
| Source note | uspto-grants-2008_04 |