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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261928Generated: November 2, 2026

CID 406 → HCID 21321703, compound

https://huagongshe.com/reaction/261928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCID 406HCID 406—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantMethyl cyclodecanecarboxylateHCID 21321736—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 21321703HCID 21321703—

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 cyclodecanecarboxylate 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 combined organic extracts are backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled to give dimethyl 2-oxo-2-cyclodecylethylphosphonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152527
Source datasetuspto-grants-1979_05
ORD IDord-8206f6770b43473dbaa15946798af7d7
Source noteuspto-grants-1979_05