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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355662Generated: 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/2355662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium PermanganateHCID 516875—
ReactantSodium BisulfiteHCID 23665763—
Reactant1,1,3-Trihydro-4,8-dioxaperfluorononanolHCID 86668230—
SolventWaterHCID 962—
ProductMethyl 2,2,3-trifluoro-3-[1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propoxy]propanoateHCID 13172791250%

Reaction Conditions

Temperature95 °C

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 sulphuric 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754795B2
Source datasetuspto-grants-2010_07
ORD IDord-739df4646dde47e780271ff7c13d32e6
Source noteuspto-grants-2010_07