HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648662Generated: October 30, 2026
Triethyl phosphonoacetate → HCID 57102019, compound
https://huagongshe.com/reaction/648662
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 20145125 | HCID 20145125 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57102019 | HCID 57102019 | — |
Reaction Steps
A solution of 2.80 gm (12.5 m mol) of ethyl diethylphosphonoacetate in 10 ml of absolute dimethylformamide was added dropwise, at ambient temperature, to 0.60 gm (12.5 m mol) of sodium hydride (50% in oil) in 15 ml of absolute dimethylformamide. The mixture was stirred for 15 minutes (until the development of gas ceased), and then a solution of 2.4 gm (6.34 m mol) of 4-[(1-(2-piperidino-phenyl)-1-butyl)-aminocarbonylmethyl]-benzaldehyde in 10 ml of absolute dimethylformamide was added thereto dropwise. The mixture was stirred for two hours at ambient temperature, concentrated by evaporation in vacuo, and distributed between water and ether. The ether phase was dried, filtered, and then evaporated in vacuo. The evaporation residue was purified by column chromatography on silica gel [toluene/acetone (10:1)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04735959 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-236d84454152414b9e05e84bed76fb73 |
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| Source note | uspto-grants-1988_04 |
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