Dimethyl Sulfoxide → HCID 20077574, compound

HRID 1655086Notes

Reaction equation

HRID 1655086 reaction equation
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH2:11]([N:17]1[C:21]([CH2:22][OH:23])=[CH:20][N:19]=[CH:18]1)[CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].C(N(CC)CC)C>ClCCl>[CH2:11]([N:17]1[C:21]([CH:22]=[O:23])=[CH:20][N:19]=[CH:18]1)[CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]

Participants

6

Procedure

A solution of dimethyl sulphoxide (0.49 ml, 7.74 mmol) in dichloromethane (2.5 ml) was added dropwise to a solution of oxalyl chloride (0.3 ml, 3.78 mmol) in dichloromethane (15 ml) at -78° C. with stirring under argon. After effervescence had ceased (15 min), a solution of the product of step (ii) (313 mg, 1.72 mmol) in dichloromethane (7.5 ml) was added dropwise. The solution was stirred for 15 minutes before triethylamine (2.3 ml, 19 mmol) was added slowly. After a further 15 minutes the solution was allowed to warm to room temperature, stirred for 30 minutes and then quenched by the addition of a saturated aqueous solution of sodium bicarbonate (10 ml). The mixture was extracted with ethyl acetate (3×10 ml). The extracts were washed with brine (1×10 ml), dried (MgSO4) and concentrated. The residue was purified by column chromatography, eluting with 10% methanol/dichloromethane (v/v), to give 1-hexyl-imidazole-5-carboxaldehyde (280mg, 90% yield) as an oil;

Workup

  1. custom(15 min)
  2. additionwas added slowly
  3. stirringstirred for 30 minutes
  4. customquenched by the addition of a saturated aqueous solution of sodium bicarbonate (10 ml)
  5. extractionThe mixture was extracted with ethyl acetate (3×10 ml)
  6. washThe extracts were washed with brine (1×10 ml)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated
  9. customThe residue was purified by column chromatography
  10. washeluting with 10% methanol/dichloromethane (v/v)

Sources & evidence

ORD record
ord-a2bf503bc0534368887d3de1dfe4d584
Source dataset
uspto-grants-1995_04
Patent number
US05410064

Reaction notes

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