Sulfuric Acid → Diethyl 3-bromo-2,4,5-trifluorobenzoylmalonate

HRID 1761649ノート

反応式

HRID 1761649 の反応式
[Mg].[C:2]([O:10][CH2:11][CH3:12])(=[O:9])[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[Br:13][C:14]1[C:15]([F:25])=[C:16]([CH:20]=[C:21]([F:24])[C:22]=1[F:23])[C:17](Cl)=[O:18].S(=O)(=O)(O)O>C1(C)C=CC=CC=1.C(O)C.C(Cl)(Cl)(Cl)Cl>[Br:13][C:14]1[C:15]([F:25])=[C:16]([CH:20]=[C:21]([F:24])[C:22]=1[F:23])[C:17]([CH:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[C:2]([O:10][CH2:11][CH3:12])=[O:9])=[O:18]

参加物

8

反応物 4

HCID 1118Sulfuric AcidHCID 7761Diethyl MalonateHCID 5462224MagnesiumHCID 137488023-Bromo-2,4,5-trifluorobenzoyl chloride

生成物 1

HCID 13748803Diethyl 3-bromo-2,4,5-trifluorobenzoylmalonate収率 98.6%

試薬・触媒・溶媒 3

HCID 702Ethanol溶媒2 回HCID 1140Toluene溶媒2 回HCID 5943Carbon Tetrachloride溶媒

実験手順

Magnesium turnings (0.22 g) and carbon tetrachloride (0.1 ml) was added to absolute ethanol (1.5 ml). To the stirring suspension was added dropwise a solution of diethyl malonate (1.4 g) and absolute ethanol (2 ml) in toluene (6 ml) during 25 minutes at 50°-60° C. The mixture was stirred for 40 minutes, and then cooled. A solution of 3-bromo-2,4,5-trifluorobenzoyl chloride (2.27 g) in anhydrous toluene (3 ml) was added dropwise to the solution at -8°~-4.5° C. during 28 minutes. The mixture was stirred for 2 hours and then mixed with ice-chilled diluted sulfuric acid. The resulting organic layer was collected and the water layer was extracted with toluene (6 ml×4). The combined organic layer was washed with water, dried over anhydrous sodium sulfate and then concentrated to give the title compound (3.25 g) as pale yellow oil.

後処理

  1. temperaturecooled
  2. stirringThe mixture was stirred for 2 hours
  3. additionmixed with ice-
  4. customThe resulting organic layer was collected
  5. extractionthe water layer was extracted with toluene (6 ml×4)
  6. washThe combined organic layer was washed with water
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-45a5c435ce104f1bb8ff9f474d80d3b9
出典データセット
uspto-grants-1989_05
特許番号
US04826982

反応ノート

読み込み中…