Hydroquinone → 2,5-Bis(3,7-dimethyloctan-3-yl)benzene-1,4-diol

HRID 1112293Notes

Reaction equation

HRID 1112293 reaction equation
[C:1]1([CH:8]=[CH:7][C:5]([OH:6])=[CH:4][CH:3]=1)[OH:2].[CH3:9][C:10](O)([CH2:13][CH2:14][CH2:15][CH:16]([CH3:18])[CH3:17])[CH2:11][CH3:12].S(=O)(=O)(O)O>CO>[CH2:11]([C:10]([C:3]1[CH:4]=[C:5]([OH:6])[C:7]([C:10]([CH3:9])([CH2:11][CH3:12])[CH2:13][CH2:14][CH2:15][CH:16]([CH3:18])[CH3:17])=[CH:8][C:1]=1[OH:2])([CH3:9])[CH2:13][CH2:14][CH2:15][CH:16]([CH3:18])[CH3:17])[CH3:12]

Participants

5

Procedure

55 g of hydroquinone and 71.5 g of 3,7-dimethyloctan-3-ol were dissolved in 100 ml of methanol. Then, 50 ml of concentrated sulfuric acid (36 N) was added dropwise thereto under stirring and cooling so as to maintain the temperature at 40° C. or less. Subsequently, the reaction mixture was maintained at 50° to 55° C. for 4 hours. The resulting reaction mixture was added to ice-water, and extracted with 500 ml of benzene. The benzene layer was washed with water and, after drying over anhydrous sodium sulfate, benzene and unreacted 3,7-dimethyloctan-3-ol were distilled off under reduced pressure. The residual oil was chromatographed on silica gel using benzene as a developing solvent. Thus, 29.8 g of 2,5-bis(1-ethyl-1,5-dimethylhexyl)hydroquinone (the same compound as obtained in Synthesis Example 1) was first eluted, and then 15.1 g of 2-(1-ethyl-1,5-dimethylhexyl)hydroquinone was eluted.

Workup

  1. temperaturecooling so as
  2. temperatureto maintain the temperature at 40° C. or less
  3. temperatureSubsequently, the reaction mixture was maintained at 50° to 55° C. for 4 hours
  4. customThe resulting reaction mixture
  5. extractionextracted with 500 ml of benzene
  6. washThe benzene layer was washed with water
  7. dry with materialafter drying over anhydrous sodium sulfate, benzene and unreacted 3,7-dimethyloctan-3-ol
  8. distillationwere distilled off under reduced pressure
  9. customThe residual oil was chromatographed on silica gel

Sources & evidence

ORD record
ord-600b29e2d455441b921ad3408ebc94cb
Source dataset
uspto-grants-1978_10
Patent number
US04121939

Reaction notes

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