HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 22-(Nonafluorobutyl)-1-docosanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 87720095 | HCID 87720095 | — |
| Reactant | HCID 131732012 | HCID 131732012 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 22-(Nonafluorobutyl)-1-docosanol | HCID 22630497 | — |
Reaction Steps
In a similar manner to the synthesis of C4F9(CH2)17OH above, C4F9CH2CHI(CH2)20OH was treated with zinc in glacial acetic acid to afford a mixture of the reduction product alcohols and acetates as well as their corresponding olefins. The mixture was treated essentially as described above with potassium hydroxide to hydrolyze the acetate esters and finally treated with hydrogen to remove the olefinic impurities and recrystallized from hexane. Approximately 16.8 g of white solids C4F9(CH2)22OH was obtained from this process with 98% purity as confirmed by GC/MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889230B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-3f51436435e24614a3f5a9eac69d7b91 |
| Source note | uspto-grants-2014_11 |