反応式
[Br:1][CH2:2][C:3](=[O:8])[C:4]([CH3:7])([CH3:6])[CH3:5].O[C:10]1[S:14][C:13](O)=[C:12](O)[C:11]=1O>CC(C)=O>[Br-:1].[O:8]=[C:3]([C:4]([CH3:7])([CH3:6])[CH3:5])[CH2:2][S+:14]1[CH2:10][CH2:11][CH2:12][CH2:13]1参加物
4
実験手順
In a 300 ml three-necked flask, 2 g of tetrahydroxythiophene was dissolved in 20 ml of acetone. To the solution, 4.87 g of 1-bromo-3,3-dimethy 2-butanone was added dropwise while stirring. After leaving for 24 hours, the deposited white crystal was collected by filtration. The white crystal was ground to a powder, which was washed with ether. The powder was dried by a vacuum drier at 30° C. for six hours to obtain 5.15 g of 2-oxo-3,3-dimethylbutyl-thiacyclopentanium bromide (yield: 75.0%).
後処理
- customAfter leaving for 24 hours
- filtrationthe deposited white crystal was collected by filtration
- washwas washed with ether
- customThe powder was dried by a vacuum drier at 30° C. for six hours
出典と根拠
- ORDレコード
- ord-281edd52038f459f88555e5efe0d8eb4
- 出典データセット
- uspto-grants-2003_08
- 特許番号
- US06602647B2
関連ノート
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