N-bromobutanimide → Methyl 2-[2-(bromomethyl)phenyl]-2-oxoacetate

HRID 742187Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 742187
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:13])[C:9]([O:11][CH3:12])=[O:10].[Br:14]N1C(=O)CCC1=O>ClC(Cl)(Cl)Cl>[Br:14][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:13])[C:9]([O:11][CH3:12])=[O:10]

Komponenten

4

Edukt 2

HCID 67184N-bromobutanimideHCID 3768392Methyl (2-methylphenyl)(oxo)acetate

Produkt 1

HCID 14697242Methyl 2-[2-(bromomethyl)phenyl]-2-oxoacetateAusbeute 49,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 5943Carbon TetrachlorideLösungsmittel

Versuchsvorschrift

5.34 g (30 millimoles) of methyl 2-methylphenyl-glyoxylate and 5.34 g (30 millimoles) of N-bromosuccinimide in 1000 l of tetrachloromethane are exposed to a 300 W Hg vapor lamp for one hour. The organic phase is then washed once with water and three times with sodium bicarbonate solution and is dried over sodium sulfate/sodium carbonate. After the solution has been evaporated down, the crude product is chromatographed over silica gel using 1:9 methyl tert-butyl ether/n-hexane. 3.8 g (49%) of the abovementioned compound are obtained as a yellow oil.

Aufarbeitung

  1. washThe organic phase is then washed once with water and three times with sodium bicarbonate solution
  2. dry with materialis dried over sodium sulfate/sodium carbonate
  3. customAfter the solution has been evaporated down
  4. customthe crude product is chromatographed over silica gel using 1:9 methyl tert-butyl ether/n-hexane

Quellen und Nachweise

ORD-Eintrag
ord-2d8ff5b6fadc488a87f920f9f936ae98
Quelldatensatz
uspto-grants-1996_09
Patentnummer
US05554578

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