Acetaldehyde → Methyl 2-bromomethyl-2-butenoate

HRID 1088027ノート

反応式

HRID 1088027 の反応式
[C:1]([O:5][CH3:6])(=[O:4])[CH:2]=[CH2:3].[CH:7](=O)[CH3:8].S(=O)(=O)(O)O.[BrH:15]>>[Br:15][CH2:3][C:2](=[CH:7][CH3:8])[C:1]([O:5][CH3:6])=[O:4]

参加物

5

実験手順

In a manner to that of S. E. Drews, D. Emsley, et al., in J. Chem. Soc., Perkin Transaction I, pp. 2079 and 2079 (1982), an ice cooled solution of methyl acrylate (IV) (8.6 g) in conc. HBr (16.5 ml) is mixed dropwise with acetaldehyde (V) (4.4 g) and then conc. sulfuric acid (15 ml). After stirring overnight, the reaction mixture is extracted thrice with ether. The extract is washed with saturated saline, dried over MgSO4, and concentrated. The resulting residue is distilled under reduced pressure to give methyl 2-bromomethyl-2-butenoate (III) (8.59 g). 83°~85° C./10 mmHg.

後処理

  1. extractionthe reaction mixture is extracted thrice with ether
  2. washThe extract is washed with saturated saline
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated
  5. distillationThe resulting residue is distilled under reduced pressure

出典と根拠

ORDレコード
ord-a4522165b2504ffd89b9ad41a58b80ee
出典データセット
uspto-grants-1990_10
特許番号
US04960879

反応ノート

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