Bromine → Propanal, 2-bromo-3,3-dimethoxy-

HRID 1729880ノート

反応式

HRID 1729880 の反応式
C[O:2][CH:3]=[CH:4][CH:5]([O:8][CH3:9])[O:6][CH3:7].[Br:10]Br>CCOCC>[Br:10][CH:4]([CH:5]([O:8][CH3:9])[O:6][CH3:7])[CH:3]=[O:2]

参加物

4

実験手順

To a solution of 25.0 g (0.19 mole) of 1,3,3-trimethoxy- 1-propene in 75 ml of ether at 5° C is added 22.4 g (0.14 mole) of bromine (bromine color begins to persist at this point) over a period of 40 minutes. The solvent is removed in vacuo at 25° C and the colorless liquid residue is added dropwise with stirring to a mixture of 25 g of sodium bicarbonate and 80 ml of 75% v/v dioxane at 0°-5° C. Stirring is continued for 30 minutes and the mixture is extracted with 200 ml and 150 ml portions of ether. The extract is dried over magnesium sulfate, evaporated in vacuo and the residue distilled through a Vigreux head to afford 2-bromo-3,3-dimethoxypropionaldehyde, b.p. 70°-73° C/8 mm.

後処理

  1. customof 40 minutes
  2. customThe solvent is removed in vacuo at 25° C
  3. additionthe colorless liquid residue is added dropwise
  4. stirringStirring
  5. extractionthe mixture is extracted with 200 ml and 150 ml portions of ether
  6. dry with materialThe extract is dried over magnesium sulfate
  7. customevaporated in vacuo
  8. distillationthe residue distilled through a Vigreux head

出典と根拠

ORDレコード
ord-be913076584140b7b68837226d378fa2
出典データセット
uspto-grants-1976_11
特許番号
US03989812

反応ノート

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