HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452627Generated: November 1, 2026
HCID 86640029, compound → HCID 68663939, compound
https://huagongshe.com/reaction/452627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86640029 | HCID 86640029 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68663939 | HCID 68663939 | 25.2% |
Reaction Steps
To a solution of diethyl[[2-[(3-phenylpropionyl)amino]-3-pyridyl]methyl]phosphonate (13.56 g, 36.03 mmol) in toluene (150 mL) was added a suspension of tert-butoxy potassium (11.41 g, 86.47 mmol) in tetrahydrofuran (86.47 mL), and the resulting mixture was stirred at 90° C. for 1 hr. The reaction mixture was concentrated under reduced pressure, water was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=9/1-0/1) and recrystallized from hexane/ethyl acetate to give the title compound (2.02 g, yield 25%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08492378B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-cc63dac02e04494893d554ba35267628 |
|---|
| Source note | uspto-grants-2013_07 |
|---|