Iodine → HCID 20467612、化合物

HRID 1413828

反応式

HRID 1413828 の反応式
[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

9

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

  1. additionwas dropped
  2. customat 50°-55° C
  3. stirringthe reaction mixture was stirred for 30 minutes
  4. customat 50°-55° C.
  5. customThe organic layer was decanted
  6. concentrationconcentrated
  7. dissolutiondissolved in ethyl ether
  8. washThe ethereal solution was washed with water
  9. customdried
  10. concentrationconcentrated
  11. 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

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