HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843601Generated: October 28, 2026
4-Pyridinecarboxaldehyde → HCID 86654331, compound
https://huagongshe.com/reaction/1843601
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 86654330 | HCID 86654330 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86654331 | HCID 86654331 | 110% |
Reaction Steps
[(3-Nitro-phenyl)-(tetrahydro-pyran-2-yloxy)-methyl]-phosphonic acid dimethyl ester (40.7 g, 0.105 mol) was dissolved in dry THF (1 L) under nitrogen. Sodium hydride (60% suspension in mineral oil)(6.3 g, 0.158 mol, 1.5 eq) was added and the mixture was stirred for 10 minutes at room temperature. Neat 4-picolinaldehyde (10 mL, 0.105 mol, 1 eq) was then added dropwise and the mixture was heated to 60° C. and stirred at this temperature for 2.5 hours. The reaction mixture was concentrated under reduced pressure to ⅓ of the original volume and then diluted with water (500 mL). pH was adjusted to 7-8 by adding a saturated solution of NaHCO3 and the mixture was extracted with ethyl acetate (4×300 mL). The organic layer was dried over Na2SO4 and concentrated to dryness. An oil (37.7 g) was obtained, which was used without further purification in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946250B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-ffc2601364a747e2863febc4178e0fb7 |
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| Source note | uspto-grants-2015_02 |
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