Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 59449615 | HCID 59449615 | — |
| Product | HCID 59449617 | HCID 59449617 | — |
Reaction Steps
In a 100 mL 3-neck flask, 0.7146 g of piperidine (8.358 mmol) catalyst, 1.4369 g of benzaldehyde (13.543 mmol), and 10.2061 g of bis(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl) malonate (12.818 mmol) were stirred at room temperature. Throughout the reaction, both a solid and liquid were observed. After two hours, some of the liquid was removed mixed with acetone to obtain a GC sample that indicated a deficiency of benzaldehyde. Approximately 1 mL of additional benzaldehyde was added. After 24 hours, the reaction was stopped and solvent was removed on a rotary evaporator. The residue was dissolved in petroleum ether and cooled in dry ice overnight. The sample was then vacuum filtered to yield the desired white solid bis(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)2-benzylidenemalonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309376B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-c492a9ddc4974a888e636fecddbc2628 |
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| Source note | uspto-grants-2012_11 |
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