Dichloromethane → 5-Tert-butyl-2-p-tolyl-2h-pyrazole-3-carbaldehyde

HRID 598732Notes

Reaction equation

HRID 598732 reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([CH2:17][OH:18])[N:8]([C:10]2[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][CH:11]=2)[N:9]=1)([CH3:4])([CH3:3])[CH3:2].C(Cl)Cl.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>O>[C:1]([C:5]1[CH:6]=[C:7]([CH:17]=[O:18])[N:8]([C:10]2[CH:11]=[CH:12][C:13]([CH3:16])=[CH:14][CH:15]=2)[N:9]=1)([CH3:4])([CH3:2])[CH3:3]

Participants

5

Procedure

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.

Workup

  1. additionpoured into a separatory funnel
  2. customThe layers separated
  3. extractionthe aqueous layer extracted twice more with 50 mL DCM
  4. washThe combined organic layers were washed with Brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated under vacuum
  7. customto afford the crude aldehyde
  8. customThe crude material was purified by flash chromatography (0-50% EtOAc:Hexanes, silica gel)

Sources & evidence

ORD record
ord-66a3f16bafed4c31b690dd05696a526f
Source dataset
uspto-grants-2011_03
Patent number
US07897599B2

Reaction notes

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