反応式
[Mg].II.Br[C:5]1[CH:10]=[CH:9][C:8]([C:11]2([CH3:16])[O:15][CH2:14][CH2:13][O:12]2)=[CH:7][CH:6]=1.[CH2:17](Br)[CH:18]=[C:19]([CH3:21])[CH3:20].[Cl-].[NH4+]>O1CCCC1.O.BrCCBr>[CH3:16][C:11]1([C:8]2[CH:9]=[CH:10][C:5]([CH2:17][CH:18]=[C:19]([CH3:21])[CH3:20])=[CH:6][CH:7]=2)[O:15][CH2:14][CH2:13][O:12]1参加物
実験手順
To a mixture of 10.2 g of magnesium turnigns, 300 ml of tetrahydrofuran and a few pieces of iodine, was added 3.8 g of 1,2-dibromoethane with stirring under a stream of nitrogen. Additionally, a solution of 93.0 g of 2-(p-bromophenyl)-2-methyl-1,3-dioxolane dissolved in 300 ml of tetrahydrofuran was dropped while keeping the temperature at 50°-55° C. After dropping, the reaction mixture was stirred for 30 minutes, and cooled to room temperature. A solution of 66.0 g of prenyl bromide in 100 ml of tetrahydrofuran was then dropped to the reaction mixture while keeping the reaction temperature at 50°-55° C., which was allowed to stand for overnight at room temperature. A solution of 20 g of ammonium chloride in 50 ml of water was added. The organic layer was decanted, concentrated and dissolved in ethyl ether. The ethereal solution was washed with water, dried, concentrated and distilled to give 69.1 g of 2-methyl-2-(p-prenylphenyl)-1,3-dioxolane, b.p. 106-107 °C/0.10 mmHg.
後処理
- additionwas dropped
- customat 50°-55° C
- stirringthe reaction mixture was stirred for 30 minutes
- customat 50°-55° C.
- customThe organic layer was decanted
- concentrationconcentrated
- dissolutiondissolved in ethyl ether
- washThe ethereal solution was washed with water
- customdried
- concentrationconcentrated
- distillationdistilled
出典と根拠
- ORDレコード
- ord-175386732090443583e4b034005d4669
- 出典データセット
- uspto-grants-1981_02
- 特許番号
- US04251543
関連ノート
読み込み中…