Methanol → Methyl 2-bromo-3-methoxypropanoate
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
- temperatureTo the mixture, cooled in an ice bath
- customA heavy oil formed
- customwas separated from the mixture
- extractionwas extracted with chloroform
- washThe extract was washed with water
- dry with materialdried (MgSO4)
- filtrationfiltered
- temperatureThe filtrate was heated to 60° C.
- addition36.9 g of bromine was added, drop-by-drop over a 2-hour period
- temperatureThe resulting mixture was cooled to 5° C.
- concentrationconcentrated in a rotary evaporator
- 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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