Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | HCID 14302178 | HCID 14302178 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14302179 | HCID 14302179 | 71.1% |
Reaction Steps
Dimethyl methylphosphonate (5.89 g, 47.5 mmol) was dissolved in anhydrous THF (80 ml). To the resulting solution cooled to -78° C. under argon atomosphere, a solution of n-butyl lithium in hexane (1.63N, 29.1 ml, 47.5 mmol) was added and the mixture was stirred for 30 minutes. A solution of methyl 4,4-dimethylhexanoate (3.00 g, 19.0 mmol) in anhydrous THF (15 ml) was then added to the reaction mxiture at -78° C. and the mixture was stirred for 30 minutes. After warming the mixture to room temperature, acetic acid was added to neutralize the solution and a small quantity of water was then added, and concentrated. After ethyl acetate was added to the residue, the ethyl acetate layer was washed with water and with brine, dried over anhydrous magnesium sulfate, and concentrated. The residue was distilled under reduced pressure to give oily product, dimethyl 5,5-dimethyl-2-oxoheptylphosphonate (3.38 g, 13.5 mmol, 71.1%, b.p.: 120°-122° C./0.18 mmHg). The structure was confirmed by the following data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04775692 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-3f94f3d776d047d6a27038c9b2b97271 |
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| Source note | uspto-grants-1988_10 |
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