Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4,4'-Bicyclohexanone | HCID 264825 | — |
| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | HCID 59133000 | HCID 59133000 | — |
Reaction Steps
882.3 g of methoxymethyltriphenylphosphonium chloride was dispersed in 2600 mL of THF, and was cooled to −10° C. while keeping the internal temperature, 313.2 g of potassium-t-butoxide was added thereto. While keeping the internal temperature, the solution was stirred for 1 hour, and then THF (800 mL) solution containing 200.0 g of bicyclohexyl-4,4′-dione was added dropwise. While keeping the internal temperature, the solution was stirred for 1 hour, and then water was added to stop the reaction. The solvent was evaporated under reduced pressure. Then, the residue was added with hexane, was vigorously stirred, and was subjected to filtration (twice). The resultant product was mixed with the filtrate, then washed with 50% methanol aqueous solution and saturated saline in this order, and dried over anhydrous magnesium sulfate. The solvent was evaporated, to obtain 231.8 g of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07651630B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-07c725ceb1df422f875bdf27c2423580 |
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| Source note | uspto-grants-2010_01 |
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