Sodium Methoxide → 1-Ethyl-2-(methoxymethyl)-4-nitrobenzene

HRID 1413680Notes

Reaction equation

HRID 1413680 reaction equation
[CH3:1][O-:2].[Na+].Cl[CH2:5][C:6]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[CH:9]=[CH:8][C:7]=1[CH2:15][CH3:16]>CO>[CH3:1][O:2][CH2:5][C:6]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[CH:9]=[CH:8][C:7]=1[CH2:15][CH3:16]

Participants

4

Conditions

Temperature
3 °C

Procedure

Sodium methoxide is added portionwise to a solution of 150.0 g of α-chloro-2-ethyl-5-nitrotoluene in 1.15 l. of methanol maintained between 18° C. and 30° C. The mixture is refluxed for 2 hours, cooled to 3° C., and filtered. The filtrate is concentrated under vacuum and the resulting slurry shaken with saturated aqueous sodium chloride and methylene chloride. The methylene chloride layer is washed, filtered through sodium sulfate, and stirred over magnesium sulfate. The filtered solution is concentrated under vacuum to yield 133.89 g. of a dark brown liquid. The crude product is fractionated by vacuum distillation to yield a yellow liquid with boiling point 113° C. to 115° C. at 0.35 mm Hg which solidifies to light yellow prisms with mp 21.5° C. to 23.5° C.

Workup

  1. temperatureThe mixture is refluxed for 2 hours
  2. filtrationfiltered
  3. concentrationThe filtrate is concentrated under vacuum
  4. washThe methylene chloride layer is washed
  5. filtrationfiltered through sodium sulfate
  6. stirringstirred over magnesium sulfate
  7. concentrationThe filtered solution is concentrated under vacuum
  8. customto yield 133.89 g
  9. distillationThe crude product is fractionated by vacuum distillation
  10. customto yield a yellow liquid with boiling point 113° C. to 115° C. at 0.35 mm Hg which

Sources & evidence

ORD record
ord-ab6fbc9e91714dbcbe6fd102d06e7950
Source dataset
uspto-grants-1981_02
Patent number
US04251264

Reaction notes

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