Hydroquinone → 2,5-Bis(3,7-dimethyloctan-3-yl)benzene-1,4-diol
反応式
[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]参加物
実験手順
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.
後処理
- temperaturecooling so as
- temperatureto maintain the temperature at 40° C. or less
- temperatureSubsequently, the reaction mixture was maintained at 50° to 55° C. for 4 hours
- customThe resulting reaction mixture
- extractionextracted with 500 ml of benzene
- washThe benzene layer was washed with water
- dry with materialafter drying over anhydrous sodium sulfate, benzene and unreacted 3,7-dimethyloctan-3-ol
- distillationwere distilled off under reduced pressure
- customThe residual oil was chromatographed on silica gel
出典と根拠
- ORDレコード
- ord-600b29e2d455441b921ad3408ebc94cb
- 出典データセット
- uspto-grants-1978_10
- 特許番号
- US04121939
反応ノート
読み込み中…