HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848187Generated: October 25, 2026
Acetic Acid → Dimethyl 2-oxo-4-methyloctylphosphonate
https://huagongshe.com/reaction/848187
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Heptanoic acid, 3-methyl-, 1-methylpropyl ester | HCID 85980 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Dimethyl 2-oxo-4-methyloctylphosphonate | HCID 13018121 | 84% |
Reaction Steps
Under an atmosphere of nitrogen, 375 ml of a 1.33 M solution of n-butyllithium in n-hexane were added dropwise to a solution of 61.9 g of dimethyl methylphosphonate in 587 ml of tetrahydrofuran at -70° C. After stirring the mixture for one hour at -70° C., a solution of 40 g of sec-butyl 3-methylheptanoate (prepared as described in Reference Example 1) in 70 ml of tetrahydrofuran was added dropwise at -70° C., and the mixture was stirred at the same temperature for 4 hours and then stirred overnight at room temperature. The reaction mixture was then acidified with acetic acid and filtered to remove the precipitated solid, and the filtrate was concentrated under reduced pressure. The residue was diluted with ethyl acetate, washed with water and a saturated aqueous solution of sodium chloride, dried over magnesium sulphate and concentrated under reduced pressure. The residue was purified by distillation under reduced pressure to give 42 g of the title compound having the following physical characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04294849 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-a7b691bee5f24488998202b3d4e00e59 |
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| Source note | uspto-grants-1981_10 |
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