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Benzaldehyde → 5,5-Bis(bromomethyl)-2-phenyl-1,3-dioxane

HRID 2073327
ノート
印刷プレビュー

反応式

HRID 2073327 の反応式
[Br:1][CH2:2][C:3]([CH2:8][Br:9])([CH2:6][OH:7])[CH2:4][OH:5].[CH:10](=O)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.S(=O)(=O)(O)O>C1C=CC=CC=1>[Br:1][CH2:2][C:3]1([CH2:8][Br:9])[CH2:6][O:7][CH:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[O:5][CH2:4]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 240BenzaldehydeHCID 1118Sulfuric AcidHCID 186922,2-Bis(bromomethyl)-1,3-propanediol

生成物 1

HCID 218230705,5-Bis(bromomethyl)-2-phenyl-1,3-dioxane収率 88.6%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

2,2-Bis(bromomethyl)propane-1,3-diol (250 g) and benzaldehyde (110 g) were added to benzene (500 cm3) containing concentrated sulphuric acid (2 cm3) and the mixture boiled. Water was removed using a Dean Stark apparatus. After about 6 hours the reaction was complete. The mixture was cooled and the sulphuric acid neutralised by the addition of excess sodium bicarbonate. The resulting solution was filtered and the benzene removed under reduced pressure to give an oil which solidified on standing. Recrystallisation from petroleum ether gave the 1,3-dioxane (296 g) as a white solid (m.p. 66° C.).

後処理

  1. customWater was removed
  2. temperatureThe mixture was cooled
  3. additionthe sulphuric acid neutralised by the addition of excess sodium bicarbonate
  4. filtrationThe resulting solution was filtered
  5. customthe benzene removed under reduced pressure
  6. customto give an oil which
  7. customRecrystallisation from petroleum ether

出典と根拠

ORDレコード
ord-4550d0a6d92b4106909d601e2b4b7037
出典データセット
uspto-grants-1990_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04916214

反応ノート

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