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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261926Generated: November 2, 2026

CID 406 → HCID 21321719, compound

https://huagongshe.com/reaction/261926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCID 406HCID 406—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantHCID 21321726HCID 21321726—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 21321719HCID 21321719—

Reaction Steps

A solution of 49.6 g (0.40 mole) dimethyl methylphosphonate (Aldrich) in 500 ml dry tetrahydrofuran is cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution is added 188 ml of 2.34 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 18 minutes at such a rate that the reaction temperature never rises above -65°. After an additional 5 minutes stirring at -78°,25.6 g (0.20 mole) methyl 5-cyclopropylvalerate is added dropwise at a rate that keeps the reaction temperature less than -70° (20 minutes). After 1.0 hour at -78° the reaction mixture is allowed to warm to ambient temperature, neutralized with 25 ml acetic acid and rotary evaporated to a white gel. The gelatinous material is taken up in 75 ml water, the aqueous phase extracted with 100 ml portions of chloroform (3x), the cmbined organic extracts are backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled to give dimethyl 2-oxo-6-cyclopropylhexylphosphonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152527
Source datasetuspto-grants-1979_05
ORD IDord-73bf69a5cd8340bb97783f8d6e6cc696
Source noteuspto-grants-1979_05