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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | HCID 178468026 | HCID 178468026 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl (1,1-diethoxyethyl)phosphine oxide | HCID 54440250 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05952478 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-bc435b38201a44b9b4423c35391248db |
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| Source note | uspto-grants-1999_09 |
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