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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2014Generated: October 23, 2026

Sodium Chloride → Diethyl 1-methyl-5-(tetrahydropyran-2-yloxy)pentylphosphonate

https://huagongshe.com/en/reaction/2014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantMethyl iodideHCID 6328—
ReactantDiethyl 5-(tetrahydropyran-2-yloxy)pentylphosphonateHCID 19689209—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductDiethyl 1-methyl-5-(tetrahydropyran-2-yloxy)pentylphosphonateHCID 19689181—

Reaction Conditions

Temperature-70 °C

Reaction Steps

30 g (0.097 mol) of diethyl 5-(tetrahydropyran-2-yloxy)pentylphosphonate were initially introduced into 200 ml of absolute tetrahydrofuran under an argon atmosphere, cooled to -70° C. and treated with 42.8 ml (0.107 mol) of a 2.5 molar solution of butyllithium in hexane. After addition, the solution was stirred for a further 30 minutes and 15.6 g (0.11 mol) of methyl iodide were then slowly added dropwise. The mixture was stirred at -70° C. for a further 2 hours and at room temperature for 4 hours, cautiously treated with a saturated sodium chloride solution and taken up in ethyl acetate. The organic phase was washed with water and a saturated sodium chloride solution, dried over sodium sulfate and distilled in a bulb tube.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728686
Source datasetuspto-grants-1998_03
ORD IDord-8696035fa4f54687939bb64a88e38937
Source noteuspto-grants-1998_03