p-Toluenesulfonic acid → 2-Ethylhexyl syringate
反応式
[CH2:1]([CH:3]([CH2:6][CH2:7][CH2:8][CH3:9])[CH2:4][OH:5])[CH3:2].[C:10](O)(=[O:22])[C:11]1[CH:21]=[C:18]([O:19][CH3:20])[C:16]([OH:17])=[C:13]([O:14][CH3:15])[CH:12]=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[C:10]([O:5][CH2:4][CH:3]([CH2:1][CH3:2])[CH2:6][CH2:7][CH2:8][CH3:9])(=[O:22])[C:11]1[CH:12]=[C:13]([O:14][CH3:15])[C:16]([OH:17])=[C:18]([O:19][CH3:20])[CH:21]=1参加物
実験手順
To 13.2 g (0.1 mol) 2-ethyl-1-hexanol in a flask equipped with reflux condenser connected to a Dean-Stark trap was added 9.9 g (0.05 mol) syringic acid, 0.2 g p-toluenesulfonic acid and 75 ml toluene. The mixture was refluxed for 20 h. Excess alcohol and toluene were distilled off under slight vacuum. The dark liquid residue was diluted with CH2Cl2 and extracted with 2% NaHCO3 +15% aqueous NaCl followed by neutral 15% aqueous NaCl solution. The organic layer was dried with anhydrous Na2SO4 and distilled. After removal of all unreacted 2-ethylhexanol the product distilled over as a viscous, colorless liquid, b.p. 204°-209° C./4×102Pa, which crystallized on standing at room temperature to a fine white solid, mp 35°-36° C. Yield: 10.1 g, 65%.
後処理
- temperaturewith reflux condenser
- temperatureThe mixture was refluxed for 20 h
- distillationExcess alcohol and toluene were distilled off under slight vacuum
- additionThe dark liquid residue was diluted with CH2Cl2
- extractionextracted with 2% NaHCO3 +15% aqueous NaCl
- dry with materialThe organic layer was dried with anhydrous Na2SO4
- distillationdistilled
- customAfter removal of all unreacted 2-ethylhexanol the product
- distillationdistilled over as a viscous, colorless liquid, b.p. 204°-209° C./4×102Pa, which
- customcrystallized
- customon standing at room temperature to a fine white solid, mp 35°-36° C
出典と根拠
- ORDレコード
- ord-2aa03a303f4c4afb9e8741f3dcdd2ee4
- 出典データセット
- uspto-grants-1984_12
- 特許番号
- US04486179
反応ノート
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