Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hexanol | HCID 8103 | — |
| Reactant | Decane | HCID 15600 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-Decanol | HCID 8174 | — |
Reaction Steps
In an inert atmosphere, 26.8 mmol each of DBU (95 ppm H2O) and 1-hexanol (26 ppm H2O) were charged into a flame-dried flask. N-Decane (2 mL, undried) was added and was found to be miscible at room temperature; only one homogeneous liquid phase was observed. CO2 (H2O<5 ppm) was slowly bubbled through the decane/1-hexanol/DBU mixture at 1 bar overnight. The resultant mixture appeared split into two separate liquids. Argon was then bubbled through the two-phase liquid mixture for 1 h at 35° C. After 1 h, the two liquids had merged into one liquid. A schematic representation of this reversible reaction appears in FIG. 4. Similar experiments were performed with hexane in place of decane and with several alcohols (1-propanol, 1-butanol, 1-hexanol, 1-octanol, and 1-decanol) in place of 1-hexanol; similar results were obtained except that with 1-decanol, no phase split was observed even after the treatment with CO2. Miscibility data for alcohol/DBU systems is presented in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07982069B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-f379f6828d8847d58e59a664041efb63 |
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| Source note | uspto-grants-2011_07 |
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