Methyl iodide → HCID 15037140, compound

HRID 1090916Notes

Reaction equation

HRID 1090916 reaction equation
C([Li])CCC.N1[CH2:11][CH2:10][O:9][CH2:8][CH2:7]1.O1C=C[C:14]([CH:17]=[O:18])=C1.C([Li])(CC)C.Cl[Si:25]([CH2:30][CH3:31])([CH2:28][CH3:29])[CH2:26][CH3:27].IC>C1COCC1.C1CCCCC1>[CH3:7][C:8]1[O:9][C:10]([Si:25]([CH2:30][CH3:31])([CH2:28][CH3:29])[CH2:26][CH3:27])=[CH:11][C:14]=1[CH:17]=[O:18]

Participants

9

Procedure

n-Butyl lithium (a 1.6 M solution in THF; 19.0 ml, 30.4 mmol) was added to a solution of morpholine (2.67 ml, 30.4 mmol) in THF (20 ml) at -78 degrees C. under argon. After 20 minutes, 3-furaldehyde (1.8 ml, 28.9 mmol) was added, followed by s-butyl-lithium (a 1.3 M solution in cyclohexane; 23.4 ml, 30.4 mmol) after another 20 minutes. Stirring was continued for 2 hours and chlorotriethylsilane (5.1 ml, 30.4 mmol) was added. After 2 hours at -78 degrees C., s Buli (23.4 ml, 30.4 mmol) was added, followed by iodomethane (5.4 ml, 86.9 mmol) after another 2 hours. The mixture was stirred at room temperature for 15 hours and quenched with ice cold dilute hydrochloric acid. Extraction with ethyl ether and evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 10% diethyl ether/hexane to give the titled aldehyde.

Workup

  1. wait23.4 ml, 30.4 mmol) after another 20 minutes
  2. waitwas continued for 2 hours
  3. waitAfter 2 hours at -78 degrees C
  4. additionwas added
  5. stirringThe mixture was stirred at room temperature for 15 hours
  6. customquenched with ice cold dilute hydrochloric acid
  7. extractionExtraction
  8. customwith ethyl ether and evaporation of the
  9. dry with materialdried (magnesium sulfate)
  10. customextracts gave an oil, which
  11. customwas purified by flash chromatography on silica using 10% diethyl ether/hexane

Sources & evidence

ORD record
ord-9e0000a100304fac8905464a2714e260
Source dataset
uspto-grants-1992_01
Patent number
US05082954

Reaction notes

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