Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoprene | HCID 6557 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Perfluorobutane-1-sulfinic acid | HCID 596595 | — |
| Product | HCID 12905479 | HCID 12905479 | 60% |
Reaction Steps
25 g (0.088 mol) of perfluorobutanesulphinic acid were initially introduced into a 100 ml three-necked flask and cooled to 0° C. Freshly distilled isoprene was then added dropwise, in excess, during which a dropping rate of 1 drop per minute had to be maintained. After the dropwise addition, the solution was immediately poured into ice-water neutralized with NaHCO3 and extracted with ether. After drying with MgSO4, the ether extract was filtered, the ether was stripped off from the filtrate in a rotary evaporator and the residue was distilled. Perfluorobutyl 3-methyl-2-butenyl sulphone of boiling point 41° C./0.1 mm Hg was obtained as a yellowish-tinged liquid in a yield of 60 to 70% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04305885 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-9ae0c2a2b46c4e0a8867a37c8512a1c3 |
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| Source note | uspto-grants-1981_12 |
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