Isopropyl iodide → HCID 14687427, compound

HRID 1700860Notes

Reaction equation

HRID 1700860 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([OH:11])[C:7](=[CH:9][CH:10]=1)[OH:8])([O-:3])=[O:2].[H-].[Na+].I[CH:15]([CH3:17])[CH3:16]>CN(C)C=O>[CH:15]([O:8][C:7]1[CH:9]=[CH:10][C:4]([N+:1]([O-:3])=[O:2])=[CH:5][C:6]=1[OH:11])([CH3:17])[CH3:16]

Participants

5

Conditions

Temperature
0 °C

Procedure

A solution of 15.5 g of 4-nitrocatechol (100 mmol) in 200 ml of N,N-dimethylformamide is added dropwise at 0° C. to a 60% suspension of sodium hydride in oil (4.2 g, 105 mmol). At the end of the addition (1 hour), the dark red solution is stirred at 0° C. for 1.5 hours and 10.5 mnl of 2-iodopropane (105 mmol) are then added dropwise. The mixture is then brought to 80° C. and stirred for 16 hours. It is then cooled to room temperature, the solvent is evaporated off and the dark red oil is dissolved in dichloromethane (300 ml). The solution is washed with water and then with saturated aqueous sodium chloride solution, the organic phase is dried over sodium sulfate and filtered, and the solvent is evaporated off. The expected product is isolated by chromatography on a column of silica (eluent: 80/20 cyclohexane/ethyl acetate). 10.5 g of a yellow oil which solidifies are recovered:

Workup

  1. additionAt the end of the addition (1 hour)
  2. customis then brought to 80° C.
  3. stirringstirred for 16 hours
  4. temperatureIt is then cooled to room temperature
  5. customthe solvent is evaporated off
  6. dissolutionthe dark red oil is dissolved in dichloromethane (300 ml)
  7. washThe solution is washed with water
  8. dry with materialwith saturated aqueous sodium chloride solution, the organic phase is dried over sodium sulfate
  9. filtrationfiltered
  10. customthe solvent is evaporated off

Sources & evidence

ORD record
ord-0f8b78863e19402b9b3c751ba2cc3638
Source dataset
uspto-grants-2002_02
Patent number
US06350913B1

Reaction notes

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