Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Phosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl ester | HCID 11207805 | — |
| Reactant | (3,4-Dimethoxyphenyl)(4-nitrophenyl)methanone | HCID 13954267 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54164249 | HCID 54164249 | 624.4% |
Reaction Steps
10.3 g of sodium hydride with 20% paraffin oil (0.343 mol) were suspended in 350 ml of tetrahydrofuran while stirring, and 75 g of diethylphosphonoacetic acid morpholide (0.0283 mol) were added dropwise to the suspension over a period of 20 minutes while cooling with ice (internal temperature 25° C.). The mixture was allowed to react for an hour during which a clear solution was formed. 70 g (0.244 mol) of 3,4-dimethoxy-4'-nitrobenzophenone were added to this solution all at once, and the mixture was refluxed for 2 hour while stirring. The solution was then evaporated in vacuo in a rotary evaporator at 60° C., and the residue was dissolved in methylene chloride/water. The organic phase was washed with water, dried over sodium sulfate and evaporated in vacuo at 60° C. The residue was triturated with 300 ml of hot methanol. 70.4 g of the title compound were obtained in the form of a faintly beige powder (73% of theory), m.p. 149°-163° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04910200 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-fe8546b3839e4e0cb86c63b4eb23a4e9 |
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| Source note | uspto-grants-1990_03 |
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