Ethyl Bromide → Diethyl Malonate

HRID 1700835

反応式

HRID 1700835 の反応式
[CH2:1](Br)[CH3:2].[C:4]([O-:10])(=[O:9])[CH2:5][C:6]([O-:8])=[O:7].[Na+].[Na+].[OH-].[Na+].CO[C:17](C)(C)[CH3:18]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.O>[C:4]([O:10][CH2:1][CH3:2])(=[O:9])[CH2:5][C:6]([O:8][CH2:17][CH3:18])=[O:7]

参加物

7

反応条件

温度
100 °C

実験手順

In an autoclave, 10.9 g (0.1 mol) of ethyl bromide were added to a solution of 2.96 g (20 mmol) of disodium malonate and 0.64 g (2 mmol) of tetrabutylammonium bromide in 5 ml of water and 10 ml of tert-butyl methyl ether. The mixture was heated to 100° C. over a period of 30 minutes, with the pressure in the autoclave rising to 3.5 bar. After a reaction time of 3½ hours at 100° C., the mixture was cooled to room temperature and depressurized. The aqueous phase was brought from pH 4.2 to pH 5.5 using 1 M sodium hydroxide solution and extracted with tert-butyl methyl ether (2×5 ml). The combined organic phases were dried over sodium sulfate and analyzed by gas chromatography (internal standard: dimethyl succinate). The product yield was 45 percent.

後処理

  1. temperatureAfter a reaction time of 3½ hours at 100° C., the mixture was cooled to room temperature
  2. extractionextracted with tert-butyl methyl ether (2×5 ml)
  3. dry with materialThe combined organic phases were dried over sodium sulfate

出典と根拠

ORDレコード
ord-97601e19138c4f28a6fa58d6a537c536
出典データセット
uspto-grants-2002_02
特許番号
US06350898B1

関連ノート

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