Dichloromethane → 2-(3-Bromo-5-chloro-phenyl)-malonic acid dimethyl ester

HRID 1810440Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1810440
Br[C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Br:9])[CH:3]=1.[C:10]([O:17][CH3:18])(=[O:16])[CH2:11][C:12]([O:14][CH3:15])=[O:13].[H-].[Na+].C(Cl)Cl>O1CCOCC1.[Cu]Br>[CH3:15][O:14][C:12](=[O:13])[CH:11]([C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Br:9])[CH:3]=1)[C:10]([O:17][CH3:18])=[O:16]

Komponenten

7

Edukt 4

HCID 6344DichloromethaneHCID 7943Dimethyl malonateHCID 24758Sodium hydrideHCID 846761,3-Dibromo-5-chlorobenzene

Produkt 1

HCID 574588062-(3-Bromo-5-chloro-phenyl)-malonic acid dimethyl ester

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 24593copper(I) bromideKatalysatorHCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

1,3-Dibromo-5-chlorobenzene (25 g, 93 mmol), dimethyl malonate (23.4 mL, 204 mmol), and copper(I) bromide (29.2 g, 204 mmol) were combined in 1,4-dioxane (300 mL) and cooled to 0° C. Sodium hydride (60% in mineral oil; 8.2 g, 204 mmol) was added slowly, and the reaction was stirred at room temperature for 20 minutes, and then stirred at 105° C. for 4 hours. After cooling to room temperature, the mixture was worked-up with CH2Cl2 and aqueous Na4OH. The organic layer was concentrated, and the residue was purified by silica gel chromatography (0-20% EtOAc in hexanes) to give the title compound.

Aufarbeitung

  1. stirringstirred at 105° C. for 4 hours
  2. temperatureAfter cooling to room temperature
  3. concentrationThe organic layer was concentrated
  4. customthe residue was purified by silica gel chromatography (0-20% EtOAc in hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-0b3b28226926445b8a8427309a70b440
Quelldatensatz
uspto-grants-2013_01
Patentnummer
US08362044B2

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