Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | HCID 15077043 | HCID 15077043 | — |
| Reactant | HCID 19841718 | HCID 19841718 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19841705 | HCID 19841705 | 95.4% |
Reaction Steps
Under argon atmosphere, a solution of n-butyllithium in hexane (1.58N, 41.8 ml, 0.066 mol) was dropwise added to a solution of dimethyl methylphosphonate (8.2 g, 0.066 mol) in anhydrous THF (120 ml) with stirring at -78° C., and the mixture was further stirred for 30 minutes. To the mixture there was dropwise added a solution of ethyl 2-methyl-4-octynoate (5.0 g, 0.0275 mol) containing 13% of methyl 2-methyl-4-octynoate in anhydrous THF (10 ml), and the whole mixture was stirred for 30 minutes. At 0° C., acetic acid (4 ml) and water (20 ml) were added to the reaction mixture followed by concentration. After water (30 ml) was added to the residue, the mixture was extracted with ethyl acetate (50 ml×2). Ethyl acetate layers were combined, washed with water (20 ml) and with brine (20 ml), and dried over anhydrous sodium sulfate to concentrate. The residue was subjected to vacuum distillation (b.p.=127°-130° C. at 0.22 mmHg), yielding dimethyl 3-methyl-2-oxo-5-nonanylphosphonate (6.82 g, 0.026 mol, 95.4% yield) as a colorless, transparent oil. The structure of this product was confirmed by the following data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04880939 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-8776d8040948459c9b748da6a5b972cc |
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| Source note | uspto-grants-1989_11 |
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