Potassium Hydroxide → HCID 58307233, compound

HRID 448373Notes

Reaction equation

HRID 448373 reaction equation
[CH3:1][N:2]([CH3:7])[CH2:3][CH2:4][CH2:5][OH:6].[OH-].[K+].F[C:11]1[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[C:13]([O:20][CH3:21])[CH:12]=1>CCCCCCCC[N+](CCCCCCCC)(CCCCCCCC)C.[Cl-]>[CH3:21][O:20][C:13]1[CH:12]=[C:11]([CH:16]=[CH:15][C:14]=1[N+:17]([O-:19])=[O:18])[O:6][CH2:5][CH2:4][CH2:3][N:2]([CH3:7])[CH3:1]

Participants

5

Conditions

Temperature
80 °C

Procedure

3-Dimethylaminopropanol (1.45 g, 14.0 mmol) was added to a mixture of powdered KOH (0.79 g, 14.0 mmol) and Aliquat 336 (0.57 g, 1.4 mmol) and the resulting mixture was stirred for 5 minutes at 80° C. Then 4-fluoro-2-methoxy-1-nitrobenzene (2.0 g, 11.7 mmol) was added, and stirring proceeded at this temperature for 30 minutes. The mixture was cooled and partitioned between methylene chloride (80 mL) and dilute aqueous HCl (80 mL), and the organic layer was extracted with dilute aqueous HCl (2×50 mL). The combined aqueous phases were washed with methylene chloride (3×75 mL), basified (3N NaOH), and extracted with methylene chloride (3×75 mL). The combined organic extracts were washed with water (3×100 mL), dried (MgSO4), and evaporated, providing 2.1 g as a yellow oil, in 71% yield: 1H NMR (CDCl3) δ 1.98 (q, J=6.8 Hz, 6H), 2.25 (s, 6H), 2.45 (t, J=7.0 Hz, 2H), 3.74 (t, J=4.6 Hz, 4H), 3.94 (s, 3H), 4.10 (t, J=6.4 Hz, 2H), 6.48-6.53 (m, 2H), 7.99 (d, J=8.8 Hz, 1H).

Workup

  1. stirringstirring
  2. waitproceeded at this temperature for 30 minutes
  3. temperatureThe mixture was cooled
  4. custompartitioned between methylene chloride (80 mL) and dilute aqueous HCl (80 mL)
  5. extractionthe organic layer was extracted with dilute aqueous HCl (2×50 mL)
  6. washThe combined aqueous phases were washed with methylene chloride (3×75 mL)
  7. extractionextracted with methylene chloride (3×75 mL)
  8. washThe combined organic extracts were washed with water (3×100 mL)
  9. dry with materialdried (MgSO4)
  10. customevaporated
  11. customproviding 2.1 g as a yellow oil

Sources & evidence

ORD record
ord-4f29c306a603448ebf4c8dca0e25fc99
Source dataset
uspto-grants-2013_07
Patent number
US08481568B2

Reaction notes

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