Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 5371891 | HCID 5371891 | — |
Reaction Steps
An 80% dipersion of sodium hydride in oil (1.31 g, 43.5 mmol, 1.15 eq) was added portionwise (~10 min) to a solution of triethylphosphonoacetate (8.26 mL, 41.6 mmol, 1.1 eq) in dry THF (160 mL) at 0° C. After 20 min., a solution of 2-pyridinecarboxaldehyde (4.05 g, 37.8 mmol) in dry THF (80 mL) was added dropwise (20 min.) at 0° C. Dry DMSO (20 mL) was added to dissolve solids formed during the addition. After 15 min., at 0° C., the mixture was poured into a cold saturated solution of NH4Cl. The layers were separated and the aqueous phase was extracted with EtOAc (3x). The organic phase was concentrated and combined with the EtOAc extracts. Conventional aqueous workup, followed by chromatography on silica using EtOAc/hexane (1:4→1:3) as eluent afforded 5.86 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05334597 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-17ca707dec91468e9fa39044f3d63031 |
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| Source note | uspto-grants-1994_08 |
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