HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2,3,3,3-tetrafluoro-2-[1,1,2,3,3,3-hexafluoro-2-(heptafluoropropoxy)propoxy]propanoate → 1H,1H-2,5-Bis(trifluoromethyl)-3,6-dioxa-perfluorononanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2,3,3,3-tetrafluoro-2-[1,1,2,3,3,3-hexafluoro-2-(heptafluoropropoxy)propoxy]propanoate | HCID 141268 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1H,1H-2,5-Bis(trifluoromethyl)-3,6-dioxa-perfluorononanol | HCID 2736150 | — |
Reaction Steps
CF3CF2CF2OCF(CF3)CF2OCF(CF3)COF obtained in Example 2-6 is reacted with methanol in an equimolar amount in the presence of sodium fluoride to obtain CF3CF2CF2OCF(CF3)CF2OCF(CF3)COOCH3. The obtained CF3CF2CF2OCF(CF3)CF2OCF(CF3)COOCH3 is reacted with sodium borohydride in 2-propanol to obtain CF3CF2CF2OCF(CF3)CF2OCF(CF3)CH2OH. The obtained CF3CF2CF2OCF(CF3)CF2OCF(CF3)CH2OH is employed as the compound in Example 2-1 to carry out the same reaction. Further, the same reactions as in Examples 2-2 to 2-6 are carried out to obtain FSO2CF2CF2COF and CF3CF2CF2OCF(CF3)CF2OCF(CF3)COF.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781612B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-776ac407fb1f41ea800061b789e94a2b |
| Source note | uspto-grants-2010_08 |