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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N,N-dimethylaminoethanethiol hydrochloride | HCID 22036395 | — |
| Reactant | 1,4-Di(3,3,4,4,5,5,6,6,6-nonafluorohexyl) maleate | HCID 86759812 | — |
| Product | 1,4-di(3,3,4,4,5,5,6,6,6-nonafluorohexyl) 2-(N,N-dimethylaminoethanethionyl)maleate | HCID 86759811 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933101B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-71d231a652584729a570b5ad7e042ac1 |
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| Source note | uspto-grants-2005_08 |
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