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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585463Generated: October 29, 2026

Chloroform → 1,4-di(3,3,4,4,5,5,6,6,6-nonafluorohexyl) 2-(N,N-dimethylaminoethanethionyl)maleate

https://huagongshe.com/reaction/585463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-dimethylaminoethanethiol hydrochlorideHCID 22036395—
Reactant1,4-Di(3,3,4,4,5,5,6,6,6-nonafluorohexyl) maleateHCID 86759812—
Product1,4-di(3,3,4,4,5,5,6,6,6-nonafluorohexyl) 2-(N,N-dimethylaminoethanethionyl)maleateHCID 8675981154%

Reaction Conditions

Temperature60 °C

Reaction Steps

In an amount of 25.1 g (41 mmol) of 1,4-di(3,3,4,4,5,5,6,6,6-nonafluorohexyl) maleate, 6.4 g (45 mmol) of N,N-di-methylaminoethanethiol hydrochloride and 5.7 g (41 mmol) of potassium carbonate were dissolved in 60 mL of N,N-dimethylformamide and stirred at 60° C. for 4 hours. Then, the reaction mixture was added with 500 mL of chloroform and the organic phase was washed with a saturated aqueous sodium hydrogencarbonate solution. Subsequently, the organic layer was collected, and the organic solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=8:2 to 0:10 (volume ratio)) to obtain 15.8 g (yield: 54%) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933101B2
Source datasetuspto-grants-2005_08
ORD IDord-71d231a652584729a570b5ad7e042ac1
Source noteuspto-grants-2005_08