反応式
[C:1]([O:4][C:5](=[O:7])[CH3:6])(=O)[CH3:2].[CH3:8][CH2:9][CH2:10]CCC.O.N1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[C:5]([O:4][CH2:1][CH2:2][CH:17]([CH2:18][CH2:19][CH:20]=[C:9]([CH3:10])[CH3:8])[CH3:16])(=[O:7])[CH3:6]参加物
5
実験手順
To 15.6 g (0.1 mol) d1-citronellol in 20 ml of dry pyridine under nitrogen is added 11.3 ml (0.12 mol) of acetic anhydride. The reaction is stirred about 48 hours and then ice is added. After one hour, the reaction is poured into hexane and water. The organic phase is washed with 5% HCl, 2M sodium carbonate, and saturated NaCl solutions, dried over calcium sulfate and solvent removed to yield dl-citronellyl acetate.
後処理
- additionice is added
- waitAfter one hour
- washThe organic phase is washed with 5% HCl, 2M sodium carbonate, and saturated NaCl solutions
- dry with materialdried over calcium sulfate and solvent
- customremoved
出典と根拠
- ORDレコード
- ord-3ddca04c8f4a4b5885d7d10c1ae64d52
- 出典データセット
- uspto-grants-1979_06
- 特許番号
- US04158096
関連ノート
読み込み中…