Ethanol → Ethyl 2-amino-3-bromo-5-methylbenzoate

HRID 1425440

Reaktionsgleichung

Reaktionsgleichung von HRID 1425440
[NH2:1][C:2]1[C:10]([Br:11])=[CH:9][C:8]([CH3:12])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.[CH2:17](O)[CH3:18]>>[NH2:1][C:2]1[C:10]([Br:11])=[CH:9][C:8]([CH3:12])=[CH:7][C:3]=1[C:4]([O:6][CH2:17][CH3:18])=[O:5]

Komponenten

4

Edukt 3

HCID 702EthanolHCID 24386Thionyl ChlorideHCID 27744002-Amino-3-bromo-5-methylbenzoic acid

Produkt 1

HCID 54594338Ethyl 2-amino-3-bromo-5-methylbenzoateAusbeute 64 %

Versuchsvorschrift

Ethanol (10 mL) was added to 2-amino-3-bromo-5-methylbenzoic acid (1.00 g, 4.4 mmol). While the mixture was stirred, thionyl chloride (1.03 g, 8.7 mmol) was added at room temperature, followed by stirring at 80° C. overnight. The reaction solution was concentrated, and then diluted with water under ice-cooling, followed by extraction with ethyl acetate. The organic layer was washed with aqueous sodium bicarbonate solution and brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=0/10, 4/6) to obtain 715 mg of the title compound as a pale yellow solid (64%).

Aufarbeitung

  1. stirringby stirring at 80° C. overnight
  2. concentrationThe reaction solution was concentrated
  3. additiondiluted with water under ice-
  4. temperaturecooling
  5. extractionfollowed by extraction with ethyl acetate
  6. washThe organic layer was washed with aqueous sodium bicarbonate solution and brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=0/10, 4/6)

Quellen und Nachweise

ORD-Eintrag
ord-536cf4a9793244299424c2221607ffff
Quelldatensatz
uspto-grants-2015_01
Patentnummer
US08927588B2

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