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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22206Generated: October 25, 2026

Diethyl Ether → HCID 178473683, compound

https://huagongshe.com/reaction/22206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium hydrideHCID 24758—
ReactantIodide IonHCID 30165—
ReactantNeryl chlorideHCID 5874259—
ReactantHCID 178473686HCID 178473686—
SolventDimethylformamideHCID 6228—
ProductHCID 178473683HCID 178473683—

Reaction Steps

To a stirred mixture of 123 mg (5.13 mmol) of sodium hydride in 10 mL of DMF at 0° C. under argon was added 1.32 g (5.13 mmol) of Example 1, Part A [(ethoxymethylphosphinyl)methyl]phosphonic acid, diethyl ester in 5 mL of DMF dropwise over 20 minutes. The mixture was stirred for 0.5 hours and was treated with 1.00 g (3.42 mmol) of Part A iodide in 3 mL of DMF. The reaction was stirred at 0° C. for 1 hour then at room temperature for 48 hours, at which time the reaction was diluted with ether and quenched with saturated NH4Cl. The organic layer was washed with water, brine, dried (MgSO4) and evaporated to provide 1.10 g of a pale yellow oil. Flash chromatography was performed on 100 g of silica gel eluted with 49.5:49.5:1 acetone/ethyl acetate/methanol (1 liter) followed by 45:45:10 acetone/ethyl acetate/methanol. Pure product fractions were combined and evaporated to provide 600 mg (43%) of title ester as a pale yellow oil, a mixture of diastereomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428028
Source datasetuspto-grants-1995_06
ORD IDord-6a90e7ab0f284dfc9b059e1e2c7eb2d0
Source noteuspto-grants-1995_06