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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantHexanoic acid, 2-methylene-, ethyl esterHCID 3014221—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl (3-methylidene-2-oxoheptyl)phosphonateHCID 2144032869%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978229
Source datasetuspto-grants-1976_08
ORD IDord-bc832bbb7fcf4b3d8b1eaa29ee5c1f28
Source noteuspto-grants-1976_08