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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618422Generated: October 26, 2026

Methyl iodide → Dimethyl (1,1-diethoxyethyl)phosphine oxide

https://huagongshe.com/reaction/618422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 178468026HCID 178468026—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl (1,1-diethoxyethyl)phosphine oxideHCID 54440250—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of methyl(1,1-diethoxyethyl)phosphine oxide, prepared as described in EP 0 501 702 (89.3 g, 0.5 mol) in THF (900 ml) at -78° C. under an atmosphere of argon is added a solution of potassium bis(trimethylsilyl)amide (688 ml, 0.521 mol) in toluene over 15 minutes. After stirring for 1 hour at -78° C., methyl iodide (34 ml, 0.55 mol) is added over 5 minutes and stirring at -78° C. continued for 1 hour. The reaction is then quenched by the addition of a 1% solution of NaH2PO4 (450 ml) and slow warming to room temperature. Concentration gives an aqueous suspension to which dichloromethane (600 ml) is added. The organic phase is separated and washed with 1% NaH2PO4 (500 ml), followed by water (500 ml). Drying over MgSO4, concentration and purification by flash vacuum silica column chromatography (chloroform-ethanol 40:1) gives a clear oil which is distilled to give dimethyl (1,1-diethoxyethyl)phosphine oxide. b.p. 100° C. at 0.05 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05952478
Source datasetuspto-grants-1999_09
ORD IDord-bc435b38201a44b9b4423c35391248db
Source noteuspto-grants-1999_09