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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333945Generated: October 25, 2026

Diethyl methylphosphonate → HCID 86691595, compound

https://huagongshe.com/reaction/333945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl methylphosphonateHCID 12685—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-(4-quinolyl)piperazine-1-carboxylateHCID 66835834—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 86691595HCID 86691595—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Diethylmethylphosphonate (302.8 mg, 2 mmol) was dissolved in anhydrous THF (2.5 ml), the mixture was cooled to −78° C. under argon, n-butyllithium (2.11 mmol, 846 μl of a 2.5 M solution in hexane) was added dropwise with stirring. After addition was complete, stirring was continued for 20 minutes, after which ethyl 4-(4-quinolyl)piperazine-1-carboxylate (284 mg, 1 mmol) dissolved in 0.5 μl THF was added dropwise. The mixture was allowed to reach room temperature overnight with continued stirring. Glacial acetic acid (0.25 ml) and water (2 ml) was added, after which the mixture was basified with 0.1 NaOH and extracted with diethylether (2×). The organic phases were combined, washed with 5% sodium bicarbonate and water. The aqueous phases were back-extracted with diethylether after basification with 0.1 N NaOH and the combined organic phases dried over magnesium sulfate and the solvent was removed under reduced pressure to yield 271 mg (0.693 mmol, 69%). MS (ESI): m/z=392.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883791B2
Source datasetuspto-grants-2014_11
ORD IDord-35905a4a66f54338a085c9c0a7ee01a4
Source noteuspto-grants-2014_11