Aluminium lithium hydride → HCID 86662723, compound

HRID 2090948Notes

Reaction equation

HRID 2090948 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[N:9]1[CH:13]=[C:12]([CH3:14])[C:11]([C:15](OCC)=[O:16])=[N:10]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1.C1(C)C=CC=CC=1.[O-2].[O-2].[Mn+4]>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[N:9]1[CH:13]=[C:12]([CH3:14])[C:11]([CH:15]=[O:16])=[N:10]1

Participants

6

Reactant 2

HCID 21226445Aluminium lithium hydrideHCID 66693692HCID 66693692, compound2×

Product 1

HCID 86662723HCID 86662723, compoundYield 73%

Reagents, catalysts & solvents 3

HCID 178418406HCID 178418406, compoundCatalystHCID 1140TolueneSolventHCID 8028TetrahydrofuranSolvent2×

Procedure

A solution (5 mL) of ethyl 1-(2-methoxyphenyl)-4-methyl-1H-pyrazole-3-carboxylate (1.6 g) synthesized in the above-mentioned (1) in tetrahydrofuran was added to an ice-cooled solution (10 mL) of lithium aluminum hydride (0.50 g) in tetrahydrofuran. The ice bath was removed, and the reaction mixture was stirred at room temperature for 1 hr, ice-cooled again, and water (1.3 mL), 1N aqueous sodium hydroxide solution (6.5 mL) and water (1.3 mL) were successively added dropwise to quench the reaction. The residue was filtered through celite, and the filtrate was concentrated under reduced pressure to give a crude product (0.79 g) of 1-(2-methoxyphenyl)-4-methyl-1H-pyrazole-3-methanol as a pale-yellow oil. This was dissolved in toluene (20 mL), manganese dioxide (2.0 g) was added, and the mixture was heated under reflux with a Dean-Stark trap for 1 hr. The reaction mixture was allowed to cool to room temperature, and manganese dioxide was collected by filtration. The solvent was evaporated under reduced pressure to give the title object compound (0.97 g, 70%) as a yellow solid.

Workup

  1. customThe ice bath was removed
  2. temperatureice-cooled again
  3. additionwater (1.3 mL), 1N aqueous sodium hydroxide solution (6.5 mL) and water (1.3 mL) were successively added dropwise
  4. customto quench
  5. customthe reaction
  6. filtrationThe residue was filtered through celite
  7. concentrationthe filtrate was concentrated under reduced pressure
  8. customto give a crude product (0.79 g) of 1-(2-methoxyphenyl)-4-methyl-1H-pyrazole-3-methanol as a pale-yellow oil
  9. temperaturethe mixture was heated
  10. temperatureunder reflux with a Dean-Stark trap for 1 hr
  11. temperatureto cool to room temperature
  12. filtrationmanganese dioxide was collected by filtration
  13. customThe solvent was evaporated under reduced pressure

Sources & evidence

ORD record
ord-8b3bb51be9f248bf8fdae663a0b51528
Source dataset
uspto-grants-2013_05
Patent number
US08436043B2

Reaction notes

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