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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165476Generated: October 25, 2026

Sodium hydride → HCID 54164249, compound

https://huagongshe.com/reaction/1165476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantPhosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl esterHCID 11207805—
Reactant(3,4-Dimethoxyphenyl)(4-nitrophenyl)methanoneHCID 13954267—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54164249HCID 54164249624.4%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04910200
Source datasetuspto-grants-1990_03
ORD IDord-fe8546b3839e4e0cb86c63b4eb23a4e9
Source noteuspto-grants-1990_03