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Imidazole → 1-Isopropyl-1H-imidazole-2-carbaldehyde

HRID 899686
Notes
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Reaction equation

HRID 899686 reaction equation
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[Li][CH2:7][CH2:8][CH2:9]C.CN([CH:14]=[O:15])C>C1COCC1>[CH:8]([N:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:14]=[O:15])([CH3:9])[CH3:7]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 795ImidazoleHCID 6228DimethylformamideHCID 178418339Butyllithium

Product 1

HCID 100575681-Isopropyl-1H-imidazole-2-carbaldehydeYield 65.5%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
0 °C

Procedure

A solution of the imidazole (890 mg, 8.08 mmol) in THF (10 mL) under nitrogen was cooled to −78° C. and n-BuLi (2.5M in hexanes, 4.5 mL, 11.3 mmol) was added. The bright yellow solution was stirred at 0° C. for 25 minutes, then DMF (1.5 mL, 19 mmol) was added. The reaction was stirred at room temperature for one hour, then was quenched by the addition of saturated aqueous NH4Cl (10 mL). The layers were separated and the aqueous solution was extracted with EtAOc (10 mL×2). The combined organic solution was dried (Na2SO4), filtered and concentrated under reduced pressure. Purification by flash column chromatography on silica (hexane/EtOAc, 1:1) gave the aldehyde as a pale yellow solid (731 mg, 5.29 mmol, 65%). 1H NMR (CDCl3) δ 1.46 (d, 6H, J=6.6 Hz), 5.46 (septet, 1H, J=6.8 Hz), 7.29 (s, 1H), 7.31 (s, 1H), 9.81 (s, 1H).

Workup

  1. stirringThe reaction was stirred at room temperature for one hour
  2. customwas quenched by the addition of saturated aqueous NH4Cl (10 mL)
  3. customThe layers were separated
  4. extractionthe aqueous solution was extracted with EtAOc (10 mL×2)
  5. dry with materialThe combined organic solution was dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customPurification by flash column chromatography on silica (hexane/EtOAc, 1:1)

Sources & evidence

ORD record
ord-ade91d2b321b44e0b8f0d31c01d0e3ce
Source dataset
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07354932B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes