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Butanal → 2-Propyl-1,3-dioxane

HRID 73814
ノート
印刷プレビュー

反応式

HRID 73814 の反応式
[CH:1](=[O:5])[CH2:2][CH2:3][CH3:4].[CH2:6](O)[CH2:7][CH2:8][OH:9]>P(=O)(O)(O)O.O>[CH2:2]([CH:1]1[O:9][CH2:8][CH2:7][CH2:6][O:5]1)[CH2:3][CH3:4]
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 2

HCID 261ButanalHCID 104421,3-Propanediol

生成物 1

HCID 2839812-Propyl-1,3-dioxane収率 56%

試薬・触媒・溶媒 2

HCID 1004Phosphoric Acid触媒HCID 962Water溶媒

実験手順

This example illustrates the limitations of conventional synthesis methods. A 500 mL round bottom is charged with 191 g normal butyraldehyde, 101 g of 1,3-propanediol, and 4 drops 85% phosphoric acid. The round bottom is fitted with a Dean-Stark trap and condenser and the entire apparatus is placed into an electric heating mantle and brought to reflux. The aldehyde/water azeotrope condenses and separates into the trap. Heating is maintained until 24 mL of water has evolved (1 hr). The mixture is cooled and poured into a separatory funnel. The solution is washed twice with 50 mL of saturated sodium bicarbonate solution and once with 50 mL of distilled water. The organics are dried over MgSO4 and the residue distilled. A fraction collected at 150° C. is 99.6% acetal and has a mass of 95.7 g. This corresponds to a yield of 56%, lower than the yields reported in Table II.

後処理

  1. customthe limitations of conventional synthesis methods
  2. customThe round bottom is fitted with a Dean-Stark trap and condenser
  3. temperatureto reflux
  4. temperatureHeating
  5. custom(1 hr)
  6. temperatureThe mixture is cooled
  7. additionpoured into a separatory funnel
  8. washThe solution is washed twice with 50 mL of saturated sodium bicarbonate solution and once with 50 mL of distilled water
  9. dry with materialThe organics are dried over MgSO4
  10. distillationthe residue distilled
  11. customA fraction collected at 150° C.

出典と根拠

ORDレコード
ord-65d86b4b9a294a3eb4681ff2ad2ec308
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08829207B2

反応ノート

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