HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643329Generated: October 26, 2026
Methanol → Methyl 2,2,3-trifluoro-3-[1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy]propanoate
https://huagongshe.com/reaction/1643329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 1,1,3-Trihydro-4,8-dioxaperfluorononanol | HCID 86668230 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 2,2,3-trifluoro-3-[1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy]propanoate | HCID 131727912 | 50% |
Reaction Steps
A 2 liter glass flask equipped with a thermometer, reflux condenser, dropping funnel and stirrer was used. 159 g of CF3O(CF2)3OCHFCF2CH2OH, 520 g water, and 100 g sulfuric acid were added to the flask. 190 g KMnO4 were added manually to the liquid over a period of 2 hours while stirring. The reaction temperature increased to 95° C. over time. After a post reaction time of two hours, an aqueous solution of sodium bisulfite was added until a clear solution was formed. 100 g of methanol and in total 400 g of 50% aqueous sulfuric acid were added. Flash distillation of the reaction mixture resulted in a two phase distillate. Fractionation of the lower phase (120 g) gave 85.5 g of CF3O(CF2)3OCHFCF2COOCH3 (bp 34-35° C./6 mbar; yield 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08119750B2 |
|---|
| Source dataset | uspto-grants-2012_02 |
|---|
| ORD ID | ord-33629e49b3cf4aa0857485cfc303749b |
|---|
| Source note | uspto-grants-2012_02 |
|---|