1,4-Dioxane → (Z)-2,6-dimethyloct-2-ene-1,8-diol
反応式
C([O:4][CH2:5][CH2:6][C:7]([CH3:15])=[CH:8][CH2:9][CH2:10][C:11](Cl)([CH3:13])[CH3:12])(=O)C.[H][H].[O:18]1CCOCC1>[Pd]>[OH:18][CH2:12]/[C:11](=[CH:10]\[CH2:9][CH2:8][CH:7]([CH2:6][CH2:5][OH:4])[CH3:15])/[CH3:13]参加物
実験手順
1 mole of 7-chloro-3,7-dimethyl-3-octenyl acetate was dissolved into 200 milliliters of dioxane and the solution was subjected to hydrogenation reaction in a reactor containing 20 grams of activated palladium black at about 25° C. under normal pressure until hydrogen was no more absorbed. Then, the palladium black was filtered off from the reaction mixture, and dioxane was distilled off from the filtrate. To the resulting residue were added 50 milliliters of water, 200 milliliters of acetone and 10 grams of silver oxide, and the mixture was heated under reflux for 72 hours. After filtrating off precipitate contained in the reaction mixture, acetone and water were distilled off from the filtrate. By distillation of the residual liquid a fraction boiling in the temperature range of 135°-145° C./4.0mmHg was collected, whereby 0.6 mole of hydroxycitronellol was obtained.
後処理
- customthe solution was subjected to hydrogenation reaction in a reactor
- customno more absorbed
- filtrationThen, the palladium black was filtered off from the reaction mixture, and dioxane
- distillationwas distilled off from the filtrate
- additionTo the resulting residue were added 50 milliliters of water, 200 milliliters of acetone and 10 grams of silver oxide
- temperaturethe mixture was heated
- temperatureunder reflux for 72 hours
- filtrationAfter filtrating off precipitate
- distillationwere distilled off from the filtrate
- distillationBy distillation of the residual liquid a fraction
- customboiling in the temperature range of 135°-145° C./4.0mmHg
- customwas collected
出典と根拠
- ORDレコード
- ord-844177c4f8b34aab842e6d912ad051a8
- 出典データセット
- uspto-grants-1976_12
- 特許番号
- US03996303
反応ノート
読み込み中…