HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176708Generated: October 29, 2026
1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexane → HCID 102598921, compound
https://huagongshe.com/reaction/2176708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexane | HCID 67733 | — |
| Reactant | 9,10-Dibromoanthracene | HCID 68226 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 102598921 | HCID 102598921 | — |
Reaction Steps
Under a nitrogen atmosphere, 9,10-dibromoanthracene (0.6 g, 1.78 mmol) and a copper powder (1.14 g, 17.8 mmol) were added to a 200 mL reaction vessel and were dissolved in anhydrous dimethyl sulfoxide (25 mL). α,α,α-Benzotrifluoride (25 mL) and C6F13I (1.96 mL, 8.93 mmol) were added thereto and reaction was carried out at 130° C. for 4 hours. After quenching with ice-water, the reaction solution was extracted with methylene chloride. Thereafter, the obtained organic layer was dried over anhydrous sodium sulfate and then filtrated. The filtrate was subjected to solvent removal on a rotary evaporator and, thereafter, separation and purification were conducted by using column chromatography. A 9,10-bis(perfluorohexyl)anthracene was obtained as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067857B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-774624c2dc924d90bc485615de2dc96a |
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| Source note | uspto-grants-2015_06 |
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