HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 5-Tert-butyl-2-p-tolyl-2h-pyrazole-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | (5-Tert-butyl-2-p-tolyl-2h-pyrazol-3-yl)-methanol | HCID 67091382 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Tert-butyl-2-p-tolyl-2h-pyrazole-3-carbaldehyde | HCID 57418555 | 98.3% |
Reaction Steps
To a scintillation vial containing (5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-methanol (0.515 g, 2.1 mmol) was added 15 mL DCM followed by the addition of Dess-Martin periodinane (1.1 g, 2.52 mmol). The reaction mixture was allowed to stir at room temperature for 20 minutes and poured into a separatory funnel containing 30 mL water. The layers separated and the aqueous layer extracted twice more with 50 mL DCM. The combined organic layers were washed with Brine, dried over MgSO4 and concentrated under vacuum to afford the crude aldehyde. The crude material was purified by flash chromatography (0-50% EtOAc:Hexanes, silica gel) to yield the desired product as a clear oil (0.5 g, 97%). Expected mass=242. Observed mass=243.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897599B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-66a3f16bafed4c31b690dd05696a526f |
| Source note | uspto-grants-2011_03 |