Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | HCID 15099539 | HCID 15099539 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21471506 | HCID 21471506 | 92% |
Reaction Steps
t-Butanol (175 mg, 2.35 mmol) was added to a stirring solution of Dess-Martin periodinane (1.005 gm, 2.37 mmol) in dry CH3CN (15 ml). After 15 minutes, a solution of 2-(4-fluorophenyl)-4-(1-methylethyl)-6-phenyl-3-pyridinemethanol (582 mg, 1.81 mmol) in CH3CN (9 ml) and CH2Cl2 (3 ml) was added to the mixture and stirring was continued for 40 minutes. The mixture was diluted with Et2O and quenched with 1N NaOH (25 ml). After 25 minutes of rapid mixing, the biphasic mixture was separated and the aqueous layer was extracted with Et2O. The combined organic layers were washed in succession with 1N NaOH, H2O, and brine, then dried (Na2SO4), filtered and stripped to yield a solid residue. The residue was chromatographed (Merck SiO2, 30% hexane in CH2Cl2) to give 2-(4-fluorophenyl)-4-(1-methylethyl)- 6-phenyl-3-pyridinecarboxaldehyde as a white solid (532 mg, 92%). An analytical sample was obtained by recrystallization from a minimum amount of hot hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05506219 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-bc6d26558f6e4ccfa236030fbaee618f |
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| Source note | uspto-grants-1996_04 |
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