HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741011Generated: November 2, 2026
Diethyl benzylphosphonate → HCID 14590315, compound
https://huagongshe.com/reaction/1741011
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl benzylphosphonate | HCID 14122 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Pyridinecarboxaldehyde, 2-amino- | HCID 737633 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14590315 | HCID 14590315 | 40.4% |
Reaction Steps
In 35 ml of tetrahydrofuran (THF) was dissolved 1.28 g of 2-aminonicotinaldehyde, followed by addition of 2.50 g of diethyl benzylphosphonate and 2.08 g of potassium hydroxide, and the mixture was refluxed at 80° C. for 4.5 hours. This reaction mixture was filtered to remove insoluble matter and the filtrate was evaporated under reduced pressure. The residue was dissolved in 2N-hydrochloric acid and the solution was washed with ether, made basic bv adding 15% aqueous sodium hydroxide solution, and extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate and the solvent was evaporated off. The residue was recrystallized from acetonitrile to provide 0.83 g of the title compound as yellow prisms. This product was used as a starting material without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05972976 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-87fc2d0942374b7b90b569003d98d873 |
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| Source note | uspto-grants-1999_10 |
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