Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexane | HCID 67733 | — |
| Reactant | Sodium dithionate | HCID 146045 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178527447 | HCID 178527447 | 67.7% |
Reaction Steps
1-Iodoperfluorohexane (89.2 g, 0.2 mol) was added rapidly to a stirred mixture of 16.8 g (0.2 mol) of sodium bicarbonate, 418 g (0.24 mol) sodium dithionate, 60 mL of water and 60 mL of acetonitrile at room temperature. After 1.5 hr, the mixture was heated to 55° C. and maintained for 4 hr. The mixture was then concentrated on a rotary evaporator to remove the acetonitrile. Ethyl acetate (250 mL) was added and the mixture was faltered. The solid was dissolved in an additional 200 mL of ethyl acetate. The combined ethyl acetate solutions were washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and concentrated on a rotary evaporator. The solid residue was recrystallized three times from 350 mL of isopropanol to give in two crops 55 g of white solid. 19F NMR (CDCl3) -80.6 (3F), -121.6 (2F), -122.2 (2F), -122.4 (2F), -125.7 (2F), -130.7 (2F).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05639837 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-97d14cad048c42feae54c89b09b54916 |
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| Source note | uspto-grants-1997_06 |
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