Methanol → Methyl 2-bromo-3-methoxypropanoate

HRID 1262459ノート

反応式

HRID 1262459 の反応式
[C:1]([O:5][CH3:6])(=[O:4])[CH:2]=[CH2:3].[Br-:7].[K+].[CH3:9][OH:10]>O>[Br:7][CH:2]([CH2:3][O:10][CH3:9])[C:1]([O:5][CH3:6])=[O:4]

参加物

5

実験手順

480 g of mercuric acetate was added to a solution of 139 g of methyl acrylate in 170 ml of methanol. The resulting mixture was stirred for 3 days at room temperature. To the mixture, cooled in an ice bath, a solution of 100 g of potassium bromide in 600 ml of water was added. A heavy oil formed, was separated from the mixture and was extracted with chloroform. The extract was washed with water, dried (MgSO4) and filtered. The filtrate was heated to 60° C. and 36.9 g of bromine was added, drop-by-drop over a 2-hour period. The resulting mixture was cooled to 5° C. and concentrated in a rotary evaporator. The liquid residue was distilled to give methyl 2-bromo-3-methoxypropionate (5A), b.p.: 69-72° C. (3-5 Torr.).

後処理

  1. temperatureTo the mixture, cooled in an ice bath
  2. customA heavy oil formed
  3. customwas separated from the mixture
  4. extractionwas extracted with chloroform
  5. washThe extract was washed with water
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. temperatureThe filtrate was heated to 60° C.
  9. addition36.9 g of bromine was added, drop-by-drop over a 2-hour period
  10. temperatureThe resulting mixture was cooled to 5° C.
  11. concentrationconcentrated in a rotary evaporator
  12. distillationThe liquid residue was distilled

出典と根拠

ORDレコード
ord-32c209c45218467794077096b67d97dc
出典データセット
uspto-grants-1984_06
特許番号
US04452626

反応ノート

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