HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284313Generated: October 28, 2026
Acetic Acid → Dimethyl (3-methylidene-2-oxoheptyl)phosphonate
https://huagongshe.com/reaction/1284313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Hexanoic acid, 2-methylene-, ethyl ester | HCID 3014221 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl (3-methylidene-2-oxoheptyl)phosphonate | HCID 21440328 | 69% |
Reaction Steps
A 2N solution (400 ml.) of n-butyllithium in diethyl ether was added dropwise to a solution of dimethyl methylphosphonate (110 g.) in pure anhydrous tetrahydrofuran (700 ml.) with stirring under nitrogen, while the reaction temperature was kept within the range of -50° to -60°C. After 10 minutes, a solution of ethyl 2-n-butylacrylate (prepared as described in (1) above; 60 g.) in tetrahydrofuran (150 ml.) was added dropwise to the reaction mixture at -65° to -70°C. and stirred for 4 hours at the same temperature. The reaction mixture was further stirred overnight at 0°C, acidified with acetic acid and concentrated under reduced pressure. Diethyl ether and water were added to the residue in order to remove the water soluble materials. The ethereal solution was dried over magnesium sulphate and concentrated. The residue was distilled under reduced pressure to give pure dimethyl 2-oxo-3-methylene-n-heptylphosphonate (67 g; 69%), having the following physical characteristics:-
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03978229 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-bc832bbb7fcf4b3d8b1eaa29ee5c1f28 |
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| Source note | uspto-grants-1976_08 |
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