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Ethanol → 4-Amino-5-fluoro-2-methoxybenzoic acid

HRID 630410
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 630410
[NH2:1][C:2]1[C:9]([F:10])=[CH:8]C(C#N)=[C:4]([O:11][CH3:12])[CH:3]=1.[OH-:13].[Na+].[CH2:15]([OH:17])[CH3:16]>>[NH2:1][C:2]1[C:9]([F:10])=[CH:8][C:16]([C:15]([OH:13])=[O:17])=[C:4]([O:11][CH3:12])[CH:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 185196344-Amino-5-fluoro-2-methoxybenzonitrile2×

Produkt 1

HCID 674693384-Amino-5-fluoro-2-methoxybenzoic acidAusbeute 80 %

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

To a solution of 4-amino-5-fluoro-2-methoxybenzonitrile (intermediate 88; 5.3 g, 0.03 mol) in ethanol (20 mL) was added sodium hydroxide 8M (27.9 mL, 0.22 mol), the mixture was placed in a sealed vessel and heated to 110° C. for 20 hours. The solvent was removed under reduced pressure and the crude obtained was partitioned between water and ether. The aqueous layer was acidified by hydrochloric acid 6N until pH 4 and the crude was extracted with ethyl acetate, dried, filtered and evaporated under reduced pressure giving the title compound as a yellow solid (80%), which was used in the next step without further purification.

Aufarbeitung

  1. customthe mixture was placed in a sealed vessel
  2. customThe solvent was removed under reduced pressure
  3. customthe crude obtained
  4. customwas partitioned between water and ether
  5. extractionthe crude was extracted with ethyl acetate
  6. customdried
  7. filtrationfiltered
  8. customevaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-b494ab6197e44209931d40c7e221138b
Quelldatensatz
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09315463B2

Notizen zur Reaktion

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