Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Propanal | HCID 527 | — |
| Reactant | Ethyl ketone | HCID 7288 | — |
| Reactant | Butyl Acetate | HCID 31272 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Catalyst | Titanium | HCID 23963 | — |
| Product | HCID 69286184 | HCID 69286184 | — |
Reaction Steps
In a bottom round flask equipped with a mechanical stirrer, a dropping funnel and a reflux condenser were loaded 265 g (3.08 mol) of the diethyl ketone with 252 g of butylacetate as the solvent, 0.36 molar equivalents of anhydrous magnesium chloride and the aforementioned titanium catalytic solution containing 0.053 molar equivalents of the trichloropropoxytitanium complex. The resulting suspension was stirred vigorously and allowed to heat to 85° C. Then 2.1 molar equivalents of propionaldehyde were added dropwise over 2 h at 85° C. The reaction was continued for an additional hour and cooled to 40° C. The reaction mixture was hydrolyzed with a 10% aqueous acetic acid solution (500 g), decanted and washed with a 10% aqueous acetic acid solution (200 g) and 50 g of NaCl. The organic phase was then washed twice with a 20% aqueous potassium carbonate solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279605B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-141c4467d4064d8fb43df1ab7a2edc86 |
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| Source note | uspto-grants-2007_10 |
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