Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 8-Vinyl-1,4-dioxaspiro[4,5]decane | HCID 57598919 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 4-Ethenylcyclohexanone | HCID 543953 | 87.5% |
Reaction Steps
Sixth Step: 103.3 g of the compound (15), 86.5 g of 98% formic acid and 200 mL of toluene were added to a reactor in a nitrogen atmosphere, and stirred under refluxing and heating for 2 hours. After confirming that the reaction had been completed by GC analysis, the reaction mixture was poured into and mixed with 500 mL of brine at 0° C. The mixture was separated into an organic layer and an aqueous layer by standing still, so as to attain extraction to the organic layer. The resulting organic layer was fractionated and washed with a saturated sodium bicarbonate aqueous solution and brine, followed by drying over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The resulting residue was distilled under reduced pressure to obtain 66.7 g of 4-vinylcyclohexanone (16) as a colorless transparent liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07510749B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-4bfe50ff125145438fbeea6ec4d98764 |
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| Source note | uspto-grants-2009_03 |
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