反応式
[C:1]([C:6]1[CH:11]=[C:10]([C:12]([CH2:15][CH3:16])([CH3:14])[CH3:13])[CH:9]=[CH:8][C:7]=1O)([CH2:4][CH3:5])([CH3:3])[CH3:2].[CH2:18](Br)[CH:19]=[CH2:20].[C:22](=[O:25])([O-])[O-].[CH3:26][C:27]([CH3:29])=O>>[C:1]([C:6]1[CH:11]=[C:10]([C:12]([CH2:15][CH3:16])([CH3:14])[CH3:13])[CH:9]=[CH:8][C:7]=1[CH:20]=[CH:19][CH2:18][O:25][CH2:22][CH:26]=[CH:27][C:29]1[CH:8]=[CH:7][C:6]([C:1]([CH2:4][CH3:5])([CH3:3])[CH3:2])=[CH:11][C:10]=1[C:12]([CH2:15][CH3:16])([CH3:14])[CH3:13])([CH2:4][CH3:5])([CH3:3])[CH3:2]参加物
5
実験手順
117.2 g of 2,4-di-t-amylphenol and 90.7 g of allylbromide was dissolved in 500 ml of acetone. Thereto was added 103.5 g of pottassium carbonate and refluxed in a water bath for 20 hours. Then reaction mixture was filtered under suction and filtration residue was rinsed with 100 ml of acetone, thereafter this was again mixed with the mother solution and then under reduced pressure acetone and excess allyl bromide was distilled out.
後処理
- temperaturerefluxed in a water bath for 20 hours
- customThen reaction mixture
- filtrationwas filtered under suction and filtration residue
- washwas rinsed with 100 ml of acetone
- additionthis was again mixed with the mother solution
- distillationunder reduced pressure acetone and excess allyl bromide was distilled out
出典と根拠
- ORDレコード
- ord-6ce65696a38043df969eb3d936abe02e
- 出典データセット
- uspto-grants-1983_12
- 特許番号
- US04421846
関連ノート
読み込み中…