Hydrochloric Acid → 1,6-Diphenylhexane
反応式
O.[C:2]1([C:8](=O)[CH2:9][CH2:10][CH2:11][CH2:12][C:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=O)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[H][H]>[Pd].O1CCCC1.C(O)C>[C:2]1([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
実験手順
In a 2-liter three-necked flask equipped with a stirring device and a nitrogen substituting device, 5 g of a Pd-C catalyst (a 5% product, containing 55.9% of water) and a solution of 100.9 g of 1,6-diphenylhexane-1,6-dione in 400 milliliters of tetrahydrofuran and 400 milliliters of denatured ethanol as well as 5 milliliters of 6N-hydrochloric acid were introduced, stirred at a normal pressure and contacted with hydrogen gas. After absorption of hydrogen was stopped, the catalyst was filtered off and the solution was concentrated. The concentrate was dissolved in ethyl acetate, washed with a dilute aqueous solution of sodium hydrogencarbonate and water, and thereafter dried with anhydrous sodium sulfate. After removing off the solvent by a rotary evaporator, a distillation under a decreased pressure was carried out, to obtain 85.3 g of 1,6-diphenylhexane as colorless liquid.
後処理
- customIn a 2-liter three-necked flask equipped with a stirring device
- additionwere introduced
- customAfter absorption of hydrogen
- filtrationthe catalyst was filtered off
- concentrationthe solution was concentrated
- dissolutionThe concentrate was dissolved in ethyl acetate
- washwashed with a dilute aqueous solution of sodium hydrogencarbonate and water
- dry with materialdried with anhydrous sodium sulfate
- customAfter removing off the solvent
- customby a rotary evaporator
- distillationa distillation under a decreased pressure
出典と根拠
- ORDレコード
- ord-ee53aaf8e1de4a32b2f39af9f74ccefb
- 出典データセット
- uspto-grants-1997_09
- 特許番号
- US05663440
反応ノート
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